N-tert-Butanesulfinyl imines in the asymmetric synthesis of nitrogen-containing heterocycles

• Joseane A. Mendes,
• Paulo R. R. Costa,
• Miguel Yus,
• Francisco Foubelo and
• Camilla D. Buarque

Beilstein J. Org. Chem. 2021, 17, 1096–1140, doi:10.3762/bjoc.17.86

• t-BuOH and LiBr as additives [102]. The isopropyl-substituted derivative 84 was easily converted into the corresponding methylene lactam 85, upon removal of the sulfinyl unit under acidic conditions. Finally, ozonolysis of 85 yielded tetramic acid 86 in 60% yield (Scheme 26). The configuration of

Synthetic accesses to biguanide compounds

• Oleksandr Grytsai,
• Cyril Ronco and
• Rachid Benhida

Beilstein J. Org. Chem. 2021, 17, 1001–1040, doi:10.3762/bjoc.17.82

• derivatives were 2 equivalents of dicyandiamide and 2.2 equivalents of trimethylsilyl chloride in dry acetonitrile under MW irradiation (200–400 W) for 15 min at 140 °C. As for the work-up, the authors described that after cooling of the reaction mixture, dilution with isopropyl alcohol (3 equivalents) and

Amino- and polyaminophthalazin-1(2H)-ones: synthesis, coordination properties, and biological activity

• Zbigniew Malinowski,
• Emilia Fornal,
• Agata Sumara,
• Renata Kontek,
• Karol Bukowski,
• Beata Pasternak,
• Dariusz Sroczyński,
• Joachim Kusz,
• Magdalena Małecka and
• Monika Nowak

Beilstein J. Org. Chem. 2021, 17, 558–568, doi:10.3762/bjoc.17.50

• selectively alkylated on the nitrogen atom [30][36]. For our purposes, the simple alkyl halides (MeI, iPrI), and 2-chloro-N,N-dimethylethylamine hydrochloride and 4-(2-chloroethyl)morpholine hydrochloride, were chosen as the alkylating agents. Thus, the desired N-methyl and N-isopropyl lactams 3a,b (3a R1

• = Me, 85%; 3b R1 = iPr, 84%) were obtained by the direct alkylation of bromophthalazinone 2 with methyl or isopropyl iodide in the presence of K2CO3 in dry acetone as the solvent (conventional heating). In the similar way also the 2-aminoethyl lactams 3c (R1 = CH2CH2NMe2) and 3d (R1 = CH2CH2(morpholin

• In conclusion, we have demonstrated an efficient synthesis of 2-substituted (alkyl, aminoalkyl) 4-aminophthalazinones 5 and 6 via the direct bromination of phthalazin-1(2H)-one (1) with potassium tribromide, followed by the alkylation of 4-bromophthalazinone 2 with methyl iodide, isopropyl iodide or

Menthyl esterification allows chiral resolution for the synthesis of artificial glutamate analogs

• Kenji Morokuma,
• Shuntaro Tsukamoto,
• Kyosuke Mori,
• Kei Miyako,
• Ryuichi Sakai,
• Raku Irie and
• Masato Oikawa

Beilstein J. Org. Chem. 2021, 17, 540–550, doi:10.3762/bjoc.17.48

• CONFLEX, as follows. Thus, as for 21* (see Figure 7), three characteristic NOESY crosspeaks observed between isopropyl protons and methyl ester protons (MeA/MeB, MeA/MeC, MeA/HD) were found to be reasonably accounted for by the top 5 stable conformers (89.9% total population) calculated for the (2S

• , surrounded by a purple square (Figure 9), are preferably in a linear zigzag arrangement, 2) the dihedral angle of O–C–CH2–C, shown in red color, is preferably 180°, and 3) on the other hand, a steric repulsion, shown in blue color, seems to occur between the isopropyl group and the methyl ester. For the (R

• steric repulsion with the large ring C with the TFA group, the isopropyl group takes a conformation proximal to the methyl ester (see Figure 7). For 10*, with smaller size of the ring C, a conformer in which the isopropyl group and the methyl ester are separated also seems to be energetically

1,2,3-Triazoles as leaving groups in S_NAr–Arbuzov reactions: synthesis of C6-phosphonated purine derivatives

• Kārlis-Ēriks Kriķis,
• Irina Novosjolova,
• Anatoly Mishnev and
• Māris Turks

Beilstein J. Org. Chem. 2021, 17, 193–202, doi:10.3762/bjoc.17.19

• to optimize the Cl→N3 SNAr process at the purine C2 position, and that way, the isopropyl phosphonate 2b was also obtained. It is known that both chloride and azide can cleave phosphonate esters [25][26][27][28], but the chloride source would not interfere with the SNAr process at C2. Hence, we

• Supporting Information File 1). The cleavage of the ester groups in the presence of NaCl was slower than in the presence of NaN3 (Figure 1 and Table S2 in Supporting Information File 1). Further, the cleavage of the sterically bulky isopropyl ester from phosphonate 2b showed a similar pattern: 5

Facile preparation and conversion of 4,4,4-trifluorobut-2-yn-1-ones to aromatic and heteroaromatic compounds

• Takashi Yamazaki,
• Yoh Nakajima,
• Minato Iida and
• Tomoko Kawasaki-Takasuka

Beilstein J. Org. Chem. 2021, 17, 132–138, doi:10.3762/bjoc.17.14

• (that is, one of the two methyl groups in acetylacetone was formally substituted for an isopropyl or a t-Bu moiety, respectively), but no reaction was observed at all. The conjugate addition of amines to this type of ynone has already been reported [21], where the authors pointed out the significant

On the mass spectrometric fragmentations of the bacterial sesterterpenes sestermobaraenes A–C

• Anwei Hou and
• Jeroen S. Dickschat

Beilstein J. Org. Chem. 2020, 16, 2807–2819, doi:10.3762/bjoc.16.231

• originating from the isopropyl group C20–19–21 or, by involving multiple C–C bond cleavages and hydrogen rearrangements, from the C25–3–4 portion. Alternatively, a combined loss of the C8–9 moiety and one methyl group (C22, C23, C24, or C25) is possible which basically combines the fragmentations of Scheme 1A

• and Scheme 1B. The loss of the isopropyl group C20–19–21 can be achieved by an inductive cleavage of 1•+ to g1•+ followed by an α-cleavage to h1+ (Scheme 1D). Starting from c1•+, two α-cleavages with the extrusion of ethylene can lead to i1•+ that upon a third α-fragmentation with loss of the methyl

• to f2•+ (Scheme 3C). Also for compound 2 different mechanisms for the formation of the fragment ion at m/z = 297 are observed, including the loss of the isopropyl group C20–19–21 or the loss of C8–9 and one methyl group. The cleavage of the isopropyl group is possible from c2•+ by an inductive ring

Encrypting messages with artificial bacterial receptors

• Pragati Kishore Prasad,
• Naama Lahav-Mankovski,
• Leila Motiei and
• David Margulies

Beilstein J. Org. Chem. 2020, 16, 2749–2756, doi:10.3762/bjoc.16.225

• supplemented with 100 μg/mL of ampicillin at 30 °C. Then, the pre-cultured cells were diluted 1:100 in fresh LB medium supplemented with the same concentration of ampicillin, and incubated until the OD600 reached ≈0.6. In order to induce protein expression, 0.1% rhamnose and 20 μM isopropyl-β-ᴅ-1

Recent developments in enantioselective photocatalysis

• Callum Prentice,
• James Morrisson,
• Andrew D. Smith and
• Eli Zysman-Colman

Beilstein J. Org. Chem. 2020, 16, 2363–2441, doi:10.3762/bjoc.16.197

Hierarchically assembled helicates as reaction platform – from stoichiometric Diels–Alder reactions to enamine catalysis

• David Van Craen,
• Jenny Begall,
• Johannes Großkurth,
• Leonard Himmel,
• Oliver Linnenberg,
• Elisabeth Isaak and
• Markus Albrecht

Beilstein J. Org. Chem. 2020, 16, 2338–2345, doi:10.3762/bjoc.16.195

• was observed using the helicate Li4[(13b)1(2)5Ti2] as catalyst. The helicates Li4[(13c)1(2)5Ti2] and Li4[(13d)1(2)5Ti2] with an isopropyl-substituted ethylamine and a cyclic secondary amine ligand as catalytically active unit showed no conversion in the nitro-Michael reaction. Solubility problems were

Lipophilicity trends upon fluorination of isopropyl, cyclopropyl and 3-oxetanyl groups

• Benjamin Jeffries,
• Zhong Wang,
• Robert I. Troup,
• Anaïs Goupille,
• Jean-Yves Le Questel,
• Charlene Fallan,
• James S. Scott,
• Elisabetta Chiarparin,
• Jérôme Graton and
• Bruno Linclau

Beilstein J. Org. Chem. 2020, 16, 2141–2150, doi:10.3762/bjoc.16.182

• Nantes, France Medicinal Chemistry, Oncology R&D, AstraZeneca, Cambridge CB4 0WG, UK 10.3762/bjoc.16.182 Abstract A systematic comparison of lipophilicity modulations upon fluorination of isopropyl, cyclopropyl and 3-oxetanyl substituents, at a single carbon atom, is provided using directly comparable

• isopropyl substituent led to larger lipophilicity modulation compared to fluorination of the cyclopropyl substituent. Keywords: aliphatic fluorination; cyclopropane; isopropyl; isostere; lipophilicity; oxetane; Introduction The introduction of small alkyl groups onto bioactive compounds as space filling

• existing appendages is also commonly employed. For example, an isopropyl and a trifluoromethyl group have very similar volumes, but a very different shape [6]. However, even the introduction of relatively small methyl groups can impart profound consequences (“the magic methyl effect”) [7][8][9] on the

Synergy between supported ionic liquid-like phases and immobilized palladium N-heterocyclic carbene–phosphine complexes for the Negishi reaction under flow conditions

• Edgar Peris,
• Raúl Porcar,
• María Macia,
• Jesús Alcázar,
• Eduardo García-Verdugo and
• Santiago V. Luis

Beilstein J. Org. Chem. 2020, 16, 1924–1935, doi:10.3762/bjoc.16.159

• kinetic plots for this model reaction are represented in Figure 1. The NHC–Pd catalyst 4a showed a rather reduced activity (less than 10% after two hours), while the catalyst bearing isopropyl moieties at the aromatic ring (4b) displayed a significant increase in the catalytic activity, reaching 67% yield

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

• , cyclopentaoxasilinone 36a was isolated in 81% yield. A systematic study of the scope showed that unsubstituted enyne 35b only afforded the desired product in 25% yield. In contrast, isopropyl and phenyl substituted enynes yielded cyclopentaoxasilinone 36c,d in 74 and 79% yield, respectively. Furthermore, electron

One-pot synthesis of 1,3,5-triazine-2,4-dithione derivatives via three-component reactions

• Gui-Feng Kang and
• Gang Zhang

Beilstein J. Org. Chem. 2020, 16, 1447–1455, doi:10.3762/bjoc.16.120

• substrates, affording the desired products 6wa–ya in 65–81% yields. The possibility of using aliphatic aldehydes in place of aromatic aldehydes was investigated for 2 and 3a. Fortunately, the reactions carried out with isobutyraldehyde (1z) yielded 31% of the isopropyl-functionalized 6-(methylthio)-3,4

Disposable cartridge concept for the on-demand synthesis of turbo Grignards, Knochel–Hauser amides, and magnesium alkoxides

• Mateo Berton,
• Kevin Sheehan,
• Andrea Adamo and
• D. Tyler McQuade

Beilstein J. Org. Chem. 2020, 16, 1343–1356, doi:10.3762/bjoc.16.115

• study, we started selecting some of the most used organomagnesium halides in synthesis. For this purpose, a ranking of the 20 most cited ones, as measured by the citation values obtained from SciFinder, was constructed (Figure 2). Based on our analysis, methyl, ethyl, isopropyl, butyl, benzyl, and

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

• -dichloroethane. Finally, the subsequent basic hydrolysis with 6 M NaOH [39] in isopropyl alcohol [41] to remove the carbamate readily afforded the desired isoxazolidine 12 in good yield (72%). The progress of the reaction was easily followed by TLC (EtOAc), and the N-unsubstituted isoxazolidin-4-ol 12 was

• hydrolysis of the corresponding N-Troc intermediate was successfully exemplified on the 3-isopropyl-substituted derivative. We believe that the presented method will provide a fast and highly stereoselective approach towards both C-3/4-cis and C-3/4-trans isomers of 3-substituted isoxazolidin-4-ols as

• -isoxazolidine 11 (120 mg, 0.29 mmol) in isopropyl alcohol (1.2 mL), and the mixture was stirred at rt for 1 h. After the disappearance of the starting material (TLC, hexanes/EtOAc, 5:1), the solution was neutralized with HCl (6 M). Afterwards, a saturated aq NaHCO3 solution (2 mL) and solid NaCl were added, and

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

• hand, Wade et al. reported that ester 138b (R = iPr) afforded the isopropyl 3-fluorophenylalaninate (139b) as racemate in 45–50% yield [70] under similar reaction conditions (Scheme 31). 2.6. Fluorination and reductive amination of phenylpyruvate A direct fluorination of the ester derivatives of

Towards triptycene functionalization and triptycene-linked porphyrin arrays

• Gemma M. Locke,
• Keith J. Flanagan and
• Mathias O. Senge

Beilstein J. Org. Chem. 2020, 16, 763–777, doi:10.3762/bjoc.16.70

• [C11 to C16, centroid···centroid distance of 3.755(3) Å and shift distance of 1.593(5) Å] involved in a head-to-head slip plane π-stacking interaction with another triptycene molecule either side, while the third face ring iii of the triptycene exhibits C23–H23B···π interactions between the isopropyl

• three methyl groups on the TMS moiety was modelled over two position in a 55:45% occupancy. Two of the isopropyl group carbon atoms C24 and C26 were two positions in a 50:50% occupancy (see Supporting Information File 2 for full details). Crystal data for 16: C100H90N8NiZn (M =1527.87 g/mol): triclinic

Regioselectively α- and β-alkynylated BODIPY dyes via gold(I)-catalyzed direct C–H functionalization and their photophysical properties

• Takahide Shimada,
• Shigeki Mori,
• Masatoshi Ishida and
• Hiroyuki Furuta

Beilstein J. Org. Chem. 2020, 16, 587–595, doi:10.3762/bjoc.16.53

• : triisopropylsilyl group; Mes: 2,4,6-trimethylphenyl group. Top and front views of the crystal structures of (a) 4a and (b) 6b with 50% thermal ellipsoid probabilities. The isopropyl groups on the silicon atom are omitted in the front view for clarity. Partial 1H NMR spectra of (a) 1a, (b) 3a, (c) 4a, (d) 5a, and (e

A systematic review on silica-, carbon-, and magnetic materials-supported copper species as efficient heterogeneous nanocatalysts in “click” reactions

• Pezhman Shiri and
• Jasem Aboonajmi

Beilstein J. Org. Chem. 2020, 16, 551–586, doi:10.3762/bjoc.16.52

• in an aqueous medium under aerobic conditions at 70 °C (Scheme 20). In another example, GO was effectively modified with CuO nanoparticles through a facile pathway that can be seen below [83]. In the next step, GO was sonicated in isopropyl alcohol for 0.5 h to produce a black dispersion. After

Copper-catalyzed enantioselective conjugate reduction of α,β-unsaturated esters with chiral phenol–carbene ligands

• Shohei Mimura,
• Sho Mizushima,
• Yohei Shimizu and
• Masaya Sawamura

Beilstein J. Org. Chem. 2020, 16, 537–543, doi:10.3762/bjoc.16.50

• affected the stereoselectivities: Lower enantioselectivities were observed with benzyl ester 2g (Table 2, entry 8, >99% yield, 70% ee) and isopropyl ester 2h (Table 2, entry 9, >99% yield, 83% ee). In addition to the α,β-unsaturated esters, an α,β-unsaturated Weinreb amide 1i afforded the corresponding

Exploring the scope of DBU-promoted amidations of 7-methoxycarbonylpterin

• Anna R. Bockman and
• Jeffrey M. Pruet

Beilstein J. Org. Chem. 2020, 16, 509–514, doi:10.3762/bjoc.16.46

• amines to be adequately reassessed on their ease of amidation (Table 2). It was found that the reaction was most affected by an α-substitution on the amine (Table 2; products 11–13). This is in agreement with known Taft parameters which show steric effects are more pronounced for an isopropyl group

Synthesis of a dihalogenated pyridinyl silicon rhodamine for mitochondrial imaging by a halogen dance rearrangement

• Jessica Matthias,
• Thines Kanagasundaram,
• Klaus Kopka and
• Carsten S. Kramer

Beilstein J. Org. Chem. 2019, 15, 2333–2343, doi:10.3762/bjoc.15.226

• of the ester group in 2’-position, an isopropyl ester derivative; another one might be the effects of the fluorine atoms and the ester group on the HOMO energy level of the benzene moiety. Since our group is interested in PET-active near-infrared (NIR) dyes for bimodal medical imaging (PET/optical

Characterization of two new degradation products of atorvastatin calcium formed upon treatment with strong acids

• Jürgen Krauß,
• Monika Klimt,
• Markus Luber,
• Peter Mayer and
• Franz Bracher

Beilstein J. Org. Chem. 2019, 15, 2085–2091, doi:10.3762/bjoc.15.206

• /dehydration process in the side chain), treatment with conc. aqueous hydrochloric acid gave a complex, bridged molecule under C–C-bond formation of the lactone moiety with the pyrrole, migration of the isopropyl group and loss of the carboxanilide residue. The novel degradation products were characterized by

• isopropyl residue, originally located at C-2 of the pyrrole, is shifted to C-3, rendering the annulated, tetrasubstituted pyrrole 6. The structure of 6 was confirmed by X-ray crystal structure analysis. However, most likely cleavage of the carboxanilide moiety (compare formation of 7 from atorvastatin with

• , which is formed via initial acid-mediated electrophilic attack of the unsaturated lactone at C-2 of the pyrrole ring. The resulting carbenium ion should be stabilized as shown in Scheme 3 (B ↔ B’). Subsequent shift of the isopropyl group from C-2 to C-3 then would give carbenium(-iminium) ion C, which

Bipolenins K–N: New sesquiterpenoids from the fungal plant pathogen Bipolaris sorokiniana

• Chin-Soon Phan,
• Hang Li,
• Simon Kessler,
• Peter S. Solomon,
• Andrew M. Piggott and
• Yit-Heng Chooi

Beilstein J. Org. Chem. 2019, 15, 2020–2028, doi:10.3762/bjoc.15.198

• ) showed 15 distinct carbon signals, while 13C and 1H NMR data (Table 1) indicated an isopropyl unit (δC 28.3, 29.2 and 73.1; δH 1.20 and 1.24), one tertiary methyl (δC 20.1; δH 1.25), a disubstituted olefin (δC 105.7 and 155.2; δH 5.12 and 4.89) and four methines (δC 39.6, 51.1, 51.6 and 54.0; δH 1.73