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Search for "stereoselective" in Full Text gives 549 result(s) in Beilstein Journal of Organic Chemistry. Showing first 200.

Reactions of 3-aryl-1-(trifluoromethyl)prop-2-yn-1-iminium salts with 1,3-dienes and styrenes

  • Thomas Schneider,
  • Michael Keim,
  • Bianca Seitz and
  • Gerhard Maas

Beilstein J. Org. Chem. 2020, 16, 2064–2072, doi:10.3762/bjoc.16.173

Graphical Abstract
  • -(1-phenylvinyl)indene 12 through an intramolecular iminium ion-induced 1,5-cyclization. The same cyclization type together with oxidative aromatization converts dihydronaphthalenes 16 into benzo[a]fluorenes 13. The stereochemistry of 12d can be explained by a stereoselective formation of trans-3,4
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Published 24 Aug 2020

Syntheses of spliceostatins and thailanstatins: a review

  • William A. Donaldson

Beilstein J. Org. Chem. 2020, 16, 1991–2006, doi:10.3762/bjoc.16.166

Graphical Abstract
  • strategies that rely on the generation of the C-14 stereocenter by stereoselective C–N bond formation. The Jacobsen group utilized an asymmetric Cr(III)-catalyzed cycloaddition reaction [27] between (2Z,4E)-3-(triethylsilyloxy)-2,4-hexadiene (40) and the aldehyde 41 to generate the 4-silyloxydihydropyran 43
  • cleavage of the secondary triisopropylsilyl ether were prerequisites for a vanadium-catalyzed stereoselective epoxidation of the exocyclic double bond to give 90. The C-4 hydroxy group was eventually protected as a triethylsilyl ether. Through abortive attempts, Jacobsen found that the generation of the
  • with a 6:1 diastereoselectivity. The Red-Al reduction of 94, protection of the 2° alcohol, and reduction of the enoate to an allylic alcohol were prerequisites for the stereoselective 2,3-sigmatropic selenoxide rearrangement to generate 95. Further protecting group manipulation and Johnson–Lemieux
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Published 13 Aug 2020

Stereoselective Biginelli-like reaction catalyzed by a chiral phosphoric acid bearing two hydroxy groups

  • Xiaoyun Hu,
  • Jianxin Guo,
  • Cui Wang,
  • Rui Zhang and
  • Victor Borovkov

Beilstein J. Org. Chem. 2020, 16, 1875–1880, doi:10.3762/bjoc.16.155

Graphical Abstract
  • To develop new efficient stereoselective catalysts for Biginelli-like reactions, a chiral phosphoric acid bearing two hydroxy groups derived from ʟ-tartaric acid was successfully synthesized via highly regioselective transformations of enantiopure 1,1,4,4-tetraphenylbutanetetraol. The obtained
  • ) H bondings with the enolizable ketone, respectively. This rigid chiral transition-state structure favored the stereoselective attack of the enol on the imine. Once the two hydroxy groups were etherified, the loss of the rigid structure would lead to low enantioselectivity. Additionally, this
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Published 31 Jul 2020

Synthesis of the tetrasaccharide repeating unit of the O-specific polysaccharide of Azospirillum doebereinerae type strain GSF71T using linear and one-pot iterative glycosylations

  • Arin Gucchait,
  • Pradip Shit and
  • Anup Kumar Misra

Beilstein J. Org. Chem. 2020, 16, 1700–1705, doi:10.3762/bjoc.16.141

Graphical Abstract
  • the O-specific polysaccharide of Azospirillum doebereinerae type strain GSF71T in a very good yield adopting sequential glycosylation followed by removal of the p-methoxybenzyl (PMB) group in the same pot. Further, the synthetic strategy was modified by carrying out three stereoselective iterative
  • elongation C-3 hydroxy group in the ʟ-rhamnosyl thioglycoside donor 3 allowed carrying out the stereoselective glycosylation steps followed by the removal of the PMB group [25] in one pot. This was achieved by using a combination [26][27][28][29][30] of N-iodosuccinimide (NIS) and perchloric acid supported
  • repeating unit of the polysaccharide (Figure 1). The stereoselective glycosylation of compound 2 with ʟ-rhamnosyl thioglycoside 3 in the presence of a combination of NIS and HClO4-SiO2 [26][27] followed by removal of the PMB group [25] from the product in the same pot by tuning of the reaction conditions
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Published 15 Jul 2020

Pauson–Khand reaction of fluorinated compounds

  • Jorge Escorihuela,
  • Daniel M. Sedgwick,
  • Alberto Llobat,
  • Mercedes Medio-Simón,
  • Pablo Barrio and
  • Santos Fustero

Beilstein J. Org. Chem. 2020, 16, 1662–1682, doi:10.3762/bjoc.16.138

Graphical Abstract
  • quantities of cobalt present in the reaction mixture. The same group also studied the intramolecular PKR of chiral fluorine-containing N-tethered 1,7-enynes 48 for the stereoselective construction of enantioenriched bicyclic alkaloid analogues 49, containing a fluorine atom in the bridge position [61]. For
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Published 14 Jul 2020

Azidophosphonium salt-directed chemoselective synthesis of (E)/(Z)-cinnamyl-1H-triazoles and regiospecific access to bromomethylcoumarins from Morita–Baylis–Hillman adducts

  • Soundararajan Karthikeyan,
  • Radha Krishnan Shobana,
  • Kamarajapurathu Raju Subimol,
  • J. Helen Ratna Monica and
  • Ayyanoth Karthik Krishna Kumar

Beilstein J. Org. Chem. 2020, 16, 1579–1587, doi:10.3762/bjoc.16.130

Graphical Abstract
  • transformations employed quaternary phosphonium salts as favourable catalysts [36]. Their synthetic utility was not only confined to catalysis, but they were also used as intermediates for the synthesis of 1H-indazoles [37], as promoters for stereoselective rearrangements [38], and as temporary protectors of O,P
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Published 01 Jul 2020

An overview on disulfide-catalyzed and -cocatalyzed photoreactions

  • Yeersen Patehebieke

Beilstein J. Org. Chem. 2020, 16, 1418–1435, doi:10.3762/bjoc.16.118

Graphical Abstract
  • . In 1996, Burton and co-workers reported the stereoselective synthesis of cis-1,2-difluorotriethylsilyethylene and its conversion to a variety of cis-1,2-difluoroethylene synthons, which are important building blocks in the preparation of fluorine-containing pharmaceuticals, polymers, and bioactive
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Published 23 Jun 2020

Recent synthesis of thietanes

  • Jiaxi Xu

Beilstein J. Org. Chem. 2020, 16, 1357–1410, doi:10.3762/bjoc.16.116

Graphical Abstract
  • ) reacted with electron-poor olefins, such as acrylonitrile (187b), methyl acrylate (187c), and cis- and trans-1,2-dichloroethenes 188, under photochemical conditions, giving 2-silylthietanes 317 and 318 in a regio- and highly stereoselective manner. However, silyl thietanes without any regio- or
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Published 22 Jun 2020

Distinctive reactivity of N-benzylidene-[1,1'-biphenyl]-2-amines under photoredox conditions

  • Shrikant D. Tambe,
  • Kwan Hong Min,
  • Naeem Iqbal and
  • Eun Jin Cho

Beilstein J. Org. Chem. 2020, 16, 1335–1342, doi:10.3762/bjoc.16.114

Graphical Abstract
  • . The developed method can be employed for the synthesis of various bulky vicinal diamines, which are potential ligands in stereoselective synthesis. Keywords: 1,2-diamine; diversity; imine; photocatalysis; visible light; Introduction The selective formation of distinct valuable compounds from the
  • applications as core structures in a variety of natural products, pharmaceuticals, and agrochemicals [34][35][36][37][38] and are valuable ligands [39][40] in stereoselective organic synthesis. Despite the availability of a plethora of synthetic methods for 1,2-diamines [41][42][43][44][45], the reported
  • electron density or position of the substituent on the benzylidene moiety. Interestingly, the homocoupling process was highly stereoselective, resulting in the formation of only one diastereomer, probably due to the bulky substitution pattern of the substrates. The structure of the homocoupled 1,2-diamine
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Published 18 Jun 2020

Highly selective Diels–Alder and Heck arylation reactions in a divergent synthesis of isoindolo- and pyrrolo-fused polycyclic indoles from 2-formylpyrrole

  • Carlos H. Escalante,
  • Eder I. Martínez-Mora,
  • Carlos Espinoza-Hicks,
  • Alejandro A. Camacho-Dávila,
  • Fernando R. Ramos-Morales,
  • Francisco Delgado and
  • Joaquín Tamariz

Beilstein J. Org. Chem. 2020, 16, 1320–1334, doi:10.3762/bjoc.16.113

Graphical Abstract
  • Chihuahua, Circuito Universitario S/N, 31125 Chihuahua, Chih., Mexico Unidad de Servicios de Apoyo en Resolución Analítica, Universidad Veracruzana, Luis Castelazo Ayala S/N, 91190 Xalapa, Ver., Mexico 10.3762/bjoc.16.113 Abstract A highly regio-, chemo- and stereoselective divergent synthesis of isoindolo
  • aromatization of the polycyclic intermediates provides the corresponding polycyclic pyrrolo-isoindoles and isoindolo-pyrrolo-indoles. A theoretical study on the stereoselective Diels–Alder reactions, carried out by calculating the endo/exo transition states, revealed the assistance of non-covalent interactions
  • (Supporting Information File 1, Table S1). Hence, the latter dienes should be more reactive than diene 8b, and consequently more stereoselective [54][55][56]. In contrast, the Gibbs energy for the diene/dienophile 8c/7b (88.8:11.2) did not completely match the experimental endo/exo (99:1) ratio, but the ZPE
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Published 17 Jun 2020

Synthesis of 3-substituted isoxazolidin-4-ols using hydroboration–oxidation reactions of 4,5-unsubstituted 2,3-dihydroisoxazoles

  • Lívia Dikošová,
  • Júlia Laceková,
  • Ondrej Záborský and
  • Róbert Fischer

Beilstein J. Org. Chem. 2020, 16, 1313–1319, doi:10.3762/bjoc.16.112

Graphical Abstract
  • of N/O-containing heterocycles used as the key intermediates in the synthesis of more complex cyclic and acyclic compounds, including various biologically active molecules. Here, we present a fast and highly stereoselective approach towards both C-3/4-cis and C-3/4-trans isomers of 3-substituted
  • isoxazolidin-4-ols. The strategy relies on a highly regio- and trans-stereoselective hydroboration–oxidation reaction of the 4,5-unsubstituted 2,3-dihydroisoxazoles with basic hydrogen peroxide. The consecutive oxidation/reduction route, sequentially employing Dess–Martin periodinane and ʟ-selectride, is used
  • hydroxylamines using malonoyl peroxide, providing N-tosylated 3-aryl-substituted 4-hydroxyisoxazolidines in a highly stereoselective manner in favor of the C-3/4-trans isomers [27]. We believe that the 3-substituted isoxazolidin-4-ols, represented by the general structures of the trans and the cis stereoisomer 3
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Published 16 Jun 2020

Ferrocenyl-substituted tetrahydrothiophenes via formal [3 + 2]-cycloaddition reactions of ferrocenyl thioketones with donor–acceptor cyclopropanes

  • Grzegorz Mlostoń,
  • Mateusz Kowalczyk,
  • André U. Augustin,
  • Peter G. Jones and
  • Daniel B. Werz

Beilstein J. Org. Chem. 2020, 16, 1288–1295, doi:10.3762/bjoc.16.109

Graphical Abstract
  • present study also demonstrated the growing potential of donor–acceptor cyclopropanes [24][25][26][27][28] as unique building blocks for current organic synthesis and especially for the efficient and highly stereoselective preparation of the relevant five-membered sulfur heterocycles derived from
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Published 10 Jun 2020

Synthesis of esters of diaminotruxillic bis-amino acids by Pd-mediated photocycloaddition of analogs of the Kaede protein chromophore

  • Esteban P. Urriolabeitia,
  • Pablo Sánchez,
  • Alexandra Pop,
  • Cristian Silvestru,
  • Eduardo Laga,
  • Ana I. Jiménez and
  • Carlos Cativiela

Beilstein J. Org. Chem. 2020, 16, 1111–1123, doi:10.3762/bjoc.16.98

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  • Chemistry Centre, Departament of Chemistry, Faculty of Chemistry and Chemical Engineering, Babeş-Bolyai University, Str. Arany Janos 11, RO-400028 Cluj−Napoca, Romania 10.3762/bjoc.16.98 Abstract The stereoselective synthesis of truxillic bis-amino esters from polyfunctional oxazolones is reported. The
  • -face arrangement, which is optimal for their [2 + 2] photocycloaddition. Irradiation of dimers 3 in CH2Cl2 solution with blue light (465 nm) promoted the chemo- and stereoselective [2 + 2] photocycloaddition of the exocyclic C=C bonds and the formation of cyclobutane-containing ortho-palladated
  • of the free species [27] and on using Pd complexes as templates [28][29][30]. The latter approach has shown good potential as a synthetic tool because it allows 1,3-diaminotruxillic derivatives to be obtained in a fully regio- and stereoselective way (only the ε-isomer is obtained). The process
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Published 25 May 2020

Palladium-catalyzed regio- and stereoselective synthesis of aryl and 3-indolyl-substituted 4-methylene-3,4-dihydroisoquinolin-1(2H)-ones

  • Valeria Nori,
  • Antonio Arcadi,
  • Armando Carlone,
  • Fabio Marinelli and
  • Marco Chiarini

Beilstein J. Org. Chem. 2020, 16, 1084–1091, doi:10.3762/bjoc.16.95

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  • (Te), Italy 10.3762/bjoc.16.95 Abstract Cascade cyclocarbopalladation of the readily available aryl/alkyl-substituted propargylic amides containing an aryl iodide moiety, followed by Suzuki–Miyaura coupling with arylboronic acids, allowed an efficient regio- and stereoselective synthesis of
  • stereoselective formation of carbon–carbon bonds [19]. Intramolecular palladium-catalyzed versions are particularly attractive, since they afford polycarbo- and heterocyclic systems via sequential reactions of the vinylpalladium intermediate [20][21][22][23][24][25]. In this field, a variety of regio- and
  • stereoselective Pd-catalyzed cascade reactions, consisting of the addition of in situ-generated arylpalladium complexes over a proximate carbon–carbon triple bond, followed by cross-coupling reactions, have been reported [26][27][28][29][30][31]. Our continuing interest in the palladium-catalyzed reactions of
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Published 20 May 2020

Copper-based fluorinated reagents for the synthesis of CF2R-containing molecules (R ≠ F)

  • Louise Ruyet and
  • Tatiana Besset

Beilstein J. Org. Chem. 2020, 16, 1051–1065, doi:10.3762/bjoc.16.92

Graphical Abstract
  • co-workers also reported the reaction of the CuCF2PO(OEt)2 reagent with α-diazocarbonyl derivatives. Depending on the copper salt used for the generation of the copper reagent, the reaction with α-diazocarbonyl derivatives provided either the α-fluorovinylphosphonate, in a stereoselective fashion, or
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Published 18 May 2020

Fluorinated phenylalanines: synthesis and pharmaceutical applications

  • Laila F. Awad and
  • Mohammed Salah Ayoup

Beilstein J. Org. Chem. 2020, 16, 1022–1050, doi:10.3762/bjoc.16.91

Graphical Abstract
  • pentafluoro-ʟ-phenylalanine derivatives 24a–c, respectively [41] (Scheme 5). The stereoselective benzylation of (S)-imidazolidinone ((S)-Boc-BMI) 25 with tetrafluorobenzyl bromides 26a,b afforded the benzylated imidazolidinones 27a,b. The acidic hydrolysis of 27a,b with simultaneous deprotection to release
  • catalytic amination of (E)-cinnamic acid The enzyme phenylalanine aminomutase (PAM) from Taxus chinensis catalyzes the stereoselective isomerization of α-phenylalanine to β-phenyalanine 111a–c. Mechanistic studies showed that (E)-cinnamic acid is an intermediate in this transformation [63]. Accordingly
  • formation [64]. 2.2. Stereoselective benzylic fluorination of N-(2-phenylacetyl)oxazolidin-2-one using NFSI Treatment of oxazolidinone 122 with N-fluorobenzenesulfonimide (NFSI) in the presence of NaHMDS afforded the fluorinated oxazolidinone derivative 123. The reductive removal of the chiral auxiliary
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Published 15 May 2020

Recent applications of porphyrins as photocatalysts in organic synthesis: batch and continuous flow approaches

  • Rodrigo Costa e Silva,
  • Luely Oliveira da Silva,
  • Aloisio de Andrade Bartolomeu,
  • Timothy John Brocksom and
  • Kleber Thiago de Oliveira

Beilstein J. Org. Chem. 2020, 16, 917–955, doi:10.3762/bjoc.16.83

Graphical Abstract
  • group publication [74] on new antimalarial drugs can be highlighted (Scheme 29). The authors report a 3.4 gram-scale preparation of ascaridole, in this case a synthetic intermediate, using TPP as photocatalyst. Another example of a scaled-up endoperoxide approach involves the stereoselective singlet
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Published 06 May 2020

Diversity-oriented synthesis of 17-spirosteroids

  • Benjamin Laroche,
  • Thomas Bouvarel,
  • Martin Louis-Sylvestre and
  • Bastien Nay

Beilstein J. Org. Chem. 2020, 16, 880–887, doi:10.3762/bjoc.16.79

Graphical Abstract
  • enyne substrates, the one-pot reaction manifold enabled the anchorage of non-steroidal spirocyclic moieties at C-17. The procedure proved efficient and stereoselective with mestranol and lynestrenol derivatives incorporating a 2-tetrahydrofuranyl spirocycle at C-17. It was more difficult with 2-oxepanyl
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Published 28 Apr 2020

Combining enyne metathesis with long-established organic transformations: a powerful strategy for the sustainable synthesis of bioactive molecules

  • Valerian Dragutan,
  • Ileana Dragutan,
  • Albert Demonceau and
  • Lionel Delaude

Beilstein J. Org. Chem. 2020, 16, 738–755, doi:10.3762/bjoc.16.68

Graphical Abstract
  • and technologies [21][22][23][24][25][26][27][28][29][30]. Thus, numerous multistep total syntheses of organic compounds, including bioactive molecules [31][32][33][34][35] and natural products [36][37], have been performed in a highly chemo- and stereoselective manner through metathesis routes [38
  • subsequent Eu(fod)3-catalyzed intermolecular Diels–Alder cycloaddition and epoxidation reactions (Scheme 5) [69]. In this stereoselective synthesis, the last biomimetic step was critical to obtain the proper enantiomer of the tetracyclic core of nanolobatolide. Amphidinolide macrolides Amphidinolides
  • metathesis in tandem with a diene cross-metathesis as the crucial steps were reported by Lee in the total synthesis of (−)-amphidinolide E (3) (Scheme 6) [70]. It is noteworthy that the second-generation Grubbs catalyst was quite active and stereoselective for both the enyne and cross-metathesis steps
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Published 16 Apr 2020

Recent advances in Cu-catalyzed C(sp3)–Si and C(sp3)–B bond formation

  • Balaram S. Takale,
  • Ruchita R. Thakore,
  • Elham Etemadi-Davan and
  • Bruce H. Lipshutz

Beilstein J. Org. Chem. 2020, 16, 691–737, doi:10.3762/bjoc.16.67

Graphical Abstract
  • )- and (E)-alkenes 311 afforded the (E)-alkene 312 as the major product. The targeted γ-borylated compounds (relative to the leaving group) were formed, each with high enantioselectivity, which can be used for further stereoselective C–C and C–X (X = heteroatom) bond formation. Catalytic Cu(NHC)-mediated
  • )boronates 320–322. High functional group tolerance and enantioselectivities are characteristics of this reaction. The stereoselective formation of a 3,3-disubstituted cyclopentene scaffold (e.g., 331), containing three contiguous asymmetric centers, was also developed starting from an achiral cyclic acetal
  • conditions, a rare cross-coupling takes place (Scheme 62) [115]. The cooperative effect of a catalytic system consisting of Cu/Ni (e.g., Ni(acac)2, CuCl, and PCy3) was also reported by Nakao et al. leading to regio- and stereoselective arylboration of 1-arylalkenes with aryl chlorides or tosylates. The
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Published 15 Apr 2020

Towards the total synthesis of chondrochloren A: synthesis of the (Z)-enamide fragment

  • Jan Geldsetzer and
  • Markus Kalesse

Beilstein J. Org. Chem. 2020, 16, 670–673, doi:10.3762/bjoc.16.64

Graphical Abstract
  • Hannover, Germany 10.3762/bjoc.16.64 Abstract The stereoselective synthesis of the (Z)-enamide fragment of chondrochloren (1) is described. A Buchwald-type coupling between amide 3 and (Z)-bromide 4 was used to generate the required fragment. The employed amide 3 comprising three chiral centers was
  • provided alcohol 11 in an excellent yield which was subjected to aminolysis to provide amide 3 in seven steps and an overall yield of 16% [16][17][18][19][20]. Synthesis of (Z)-bromide 4 For the synthesis of (Z)-bromide 4 we chose a palladium-catalyzed, stereoselective dehalogenation as the key step
  • ][19][20], whereas the (Z)-bromide 4 can be generated in a four-step sequence with a 39% overall yield, including a palladium-catalyzed, stereoselective dehalogenation [21][22][23][24][25]. Retrosynthetic analysis of chondrochlorene A (1). Synthesis of amide 3 [16][17][18][19][20]. TIPDSCl2 = 1,3
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Published 14 Apr 2020

Synthesis of disparlure and monachalure enantiomers from 2,3-butanediacetals

  • Adam Drop,
  • Hubert Wojtasek and
  • Bożena Frąckowiak-Wojtasek

Beilstein J. Org. Chem. 2020, 16, 616–620, doi:10.3762/bjoc.16.57

Graphical Abstract
  • Adam Drop Hubert Wojtasek Bozena Frackowiak-Wojtasek Institute of Chemistry, Opole University, ul. Oleska 48, 45-052 Opole, Poland ZWP EMITOR S.C., ul. Olimpijska 6, 45-681 Opole, Poland 10.3762/bjoc.16.57 Abstract 2,3-Butanediacetal derivatives were used for the stereoselective synthesis of
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Published 03 Apr 2020

Regio- and stereoselective synthesis of new ensembles of diversely functionalized 1,3-thiaselenol-2-ylmethyl selenides by a double rearrangement reaction

  • Svetlana V. Amosova,
  • Andrey A. Filippov,
  • Nataliya A. Makhaeva,
  • Alexander I. Albanov and
  • Vladimir A. Potapov

Beilstein J. Org. Chem. 2020, 16, 515–523, doi:10.3762/bjoc.16.47

Graphical Abstract
  • a regio- and stereoselective manner affording 1,3-thiaselenol-2-ylmethyl vinyl selenides in high yields predominantly with Z-configuration. Not a single representative of the 1,3-thiaselenol-2-ylmethyl selenide scaffold has been previously described in the literature. Keywords: 2-(bromomethyl)-1,3
  • -thiaselenole; nucleophilic addition; nucleophilic substitution; rearrangement; seleniranium intermediate; Introduction The regio- and stereoselective synthesis of organoselenium compounds based on selenium-centered electrophilic reagents has been one of the most important and effective directions in
  • did not occur (Scheme 2). The high anchimeric assistance effect of the selenium atom in thiaselenole 1 is the driving force for the generation of the seleniranium intermediate 2. A fundamental approach to the regio- and stereoselective synthesis of unsaturated functionalized organoselenium compounds
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Published 27 Mar 2020

Architecture and synthesis of P,N-heterocyclic phosphine ligands

  • Wisdom A. Munzeiwa,
  • Bernard Omondi and
  • Vincent O. Nyamori

Beilstein J. Org. Chem. 2020, 16, 362–383, doi:10.3762/bjoc.16.35

Graphical Abstract
  • usually lead to stereoselective reduction products, hence, they are used for the synthesis of chiral phosphines from chiral oxides [53]. Lithium tetrahydridoaluminate is used for the reduction of achiral phosphines because its action on optically active phosphine oxides leads mainly to the optically
  • precursors. However, asymmetric synthesis can be used as strategy to introduce stereogenic P-atoms into the ligand’s backbone. The borane complexation approach is a unique stereoselective way for introducing a P-stereogenic center. Benoit et al. [2] reported on the synthesis of 2-phenyl-1,3,2
  • steric properties, use of low-priced and easily available reagents, mild and expedient reaction conditions, and few reaction steps. The motifs can also be chiral, and this is helpful in stereoselective synthesis. The introduction of different moieties can bring about enhanced properties like fluorescence
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Published 12 Mar 2020

Combination of multicomponent KA2 and Pauson–Khand reactions: short synthesis of spirocyclic pyrrolocyclopentenones

  • Riccardo Innocenti,
  • Elena Lenci,
  • Gloria Menchi and
  • Andrea Trabocchi

Beilstein J. Org. Chem. 2020, 16, 200–211, doi:10.3762/bjoc.16.23

Graphical Abstract
  • possessing a Z geometry, as evinced by a NOE interaction between Hd and the methyl group. The cis relationship between the OH group and the pyrrolidine ring, resulting from the chemo- and stereoselective syn reduction of the carbonyl group, was evinced by NOESY-1D experiments showing intense NOE effects
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Published 12 Feb 2020
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