Selectfluor and alcohol-mediated synthesis of bicyclic oxyfluorination compounds by Wagner–Meerwein rearrangement

• Ziya Dağalan,
• Muhammed Hanifi Çelikoğlu,
• Saffet Çelik,
• Ramazan Koçak and
• Bilal Nişancı

Beilstein J. Org. Chem. 2024, 20, 1462–1467, doi:10.3762/bjoc.20.129

• . Keywords: alkoxyfluorine compounds; bicyclic alkene; oxyfluorination; selectfluor; Wagner–Meerwein rearrangement; Introduction Organofluorines are of great importance in the pharmaceutical and agrochemical industries, as the presence of fluorine has a serious effect on the biological activities of organic

• compounds 4a–j were also obtained in very good yields (60–98%, Scheme 2). Since the reaction mechanism proceeding with a Wagner–Meerwein rearrangement does not cause racemization or a diastereomeric mixture and preserves the initial enantiomeric excess in the camphene's fluoroalkoxy derivatives (Scheme 4

• selectfluor and a carbocation is formed by bonding with fluorine. Subsequently, fluoroalkoxy compound 4 is formed by Wagner–Meerwein rearrangement followed by alcohol addition and deprotonation. Conclusion New bicyclic fluoroalkoxy compounds were synthesized by a molecular fluorine and metal-free methodology

Exploring the role of halogen bonding in iodonium ylides: insights into unexpected reactivity and reaction control

• Carlee A. Montgomery and
• Graham K. Murphy

Beilstein J. Org. Chem. 2023, 19, 1171–1190, doi:10.3762/bjoc.19.86

• intermediate was not viable under such mild conditions. The initially proposed ionic pathway (Figure 5, left) was abandoned as solvent effects had little influence on the reaction rate, and since no Wagner–Meerwein rearrangement products were detected with bicyclic olefin precursors. Radical-based pathways

Strategies in the synthesis of dibenzo[b,f]heteropines

• David I. H. Maier,
• Barend C. B. Bezuidenhoudt and
• Charlene Marais

Beilstein J. Org. Chem. 2023, 19, 700–718, doi:10.3762/bjoc.19.51

• good yield (80%) by heating 23 in polyphosphoric acid (Scheme 5). Independently, in an effort to synthesise phenothiazine isosteres, Craig et al. [39] prepared 1a via a Wagner–Meerwein rearrangement of 23 with P2O5 (Scheme 5) the following year. The method was used to successfully synthesise

• copper-catalysed oxidative conditions to effect the transformation to 30 and 31. 2.3 Ring expansion from N-arylisatins Elliott et al. [47] reported the four-step synthesis of fluorinated 5H-dibenzo[b,f]azepine 38 from N-arylisatin 34 via Wagner–Meerwein rearrangement of 9-acridinemethanol 37 [43] (Scheme

• '-diaminobibenzyl (20). Synthesis of 10,11-dihydro-5H-dibenzo[b,f]azepine (2a) via amine condensation. Catalytic reduction of 10,11-dihydro-5H-dibenzo[b,f]azepine (2a). The Wagner–Meerwein rearrangement of acridin-9-ylmethanol (23) into 5H-dibenzo[b,f]azepine (1a). Oxidative ring expansion of 2-(9-xanthenyl

Germacrene B – a central intermediate in sesquiterpene biosynthesis

• Houchao Xu and
• Jeroen S. Dickschat

Beilstein J. Org. Chem. 2023, 19, 186–203, doi:10.3762/bjoc.19.18

• dehydration of (−)-1(10)-valencen-7β-ol (35) (Scheme 10C) [92], but has not been isolated from natural sources. Compound 22 could be formed from I1a by Wagner–Meerwein rearrangement to I1c and deprotonation (Scheme 7). This hydrocarbon ([α]D22 = +26, c 0.06) has been obtained as a dehydration product of

• through Wagner–Meerwein rearrangement to I2c and deprotonation, but also this compound is not known as a natural product. This hydrocarbon has been obtained by partial hydrogenation of (+)-α-vetispirene (49) in a small scale reaction using PtO2 hydrate in CHCl3 as a catalyst (Scheme 12F). The amounts of

• and deprotonation. However, this hydrocarbon has not been isolated from natural sources and is only known as racemic synthetic material [106]. Similarly, 52 has only been described as a synthetic compound [107]. Its hypothetical biosynthesis is possible from I3a by Wagner–Meerwein rearrangement to I3c

The enzyme mechanism of patchoulol synthase

• Houchao Xu,
• Bernd Goldfuss,
• Gregor Schnakenburg and
• Jeroen S. Dickschat

Beilstein J. Org. Chem. 2022, 18, 13–24, doi:10.3762/bjoc.18.2

• deprotonated to 6, followed by another reprotonation to F, cyclisation to G and Wagner–Meerwein rearrangement to D, the same final intermediate as suggested by Croteau. This mechanism was supported by feeding experiments with (4R)-[2-14C,4-3H]mevalonic acid (15) that is converted through IPP and DMAPP into FPP

• migration from C to D in Scheme 1A), and a Wagner–Meerwein rearrangement to G. The final steps are identical to those in Akhila’s mechanism (Scheme 2A). This work also reported on a labelling experiment with (2-2H)FPP that was enzymatically converted with PTS with incorporation of deuterium at C2 of 3

• . (Scheme 2) [10] DFT calculations have been performed previously by us as part of a general study on guaiane sesquiterpenes from germacrene A (8) [29]. After reprotonation of the neutral intermediate 6 to F the next cyclisation to G and Wagner–Meerwein rearrangement to D can be realised with low TS

All-carbon [3 + 2] cycloaddition in natural product synthesis

• Zhuo Wang and
• Junyang Liu

Beilstein J. Org. Chem. 2020, 16, 3015–3031, doi:10.3762/bjoc.16.251

• ] cycloaddition [17] of enone 95 and tert-butyl 2-butynoate (96) with PBu3 and K2CO3/MeOH as additive to give the cycloaddition adduct 97 in 83% yield [43] (Scheme 6C). A seven-step synthesis from 97 gave pentacyclic ketone 98. Pentacyclic ketone 98 was exposed to PTSA under reflux to give the Wagner–Meerwein

• rearrangement product 99 in 85% yield. The synthesis of daphenylline (11) was completed by a seven-step synthesis from benzofuran 99. Phosphine-catalyzed enantioselective [3 + 2] annulation In 2019, Lu and co-workers disclosed a novel chiral-phosphine-catalyzed enantioselective [3 + 2] annulation of allenes and

Synthetic approaches to bowl-shaped π-conjugated sumanene and its congeners

• Shakeel Alvi and
• Rashid Ali

Beilstein J. Org. Chem. 2020, 16, 2212–2259, doi:10.3762/bjoc.16.186

Synthesis of C₇₀-fragment buckybowls bearing alkoxy substituents

• Yumi Yakiyama,
• Shota Hishikawa and
• Hidehiro Sakurai

Beilstein J. Org. Chem. 2020, 16, 681–690, doi:10.3762/bjoc.16.66

• expansion by Wagner–Meerwein rearrangement, followed by Pd-catalyzed annulation (Figure 1) [18]. An UV–vis spectroscopy study revealed that the electronic character of 1 rather resembled that of an indenopyrene moiety than that of benzopyrene. Our synthetic route allows to easily introduce substituents on

• at −78 °C was treated with 150 mol % of the corresponding arylaldehydes to afford 3a and 3b quantitatively. The Wagner–Meerwein rearrangement from 3a and 3b to 4a and 4b by 100 mol % of p-TsOH in toluene under reflux conditions also occurred quantitatively. The final cyclization of 4a was carried out

One hundred years of benzotropone chemistry

• Arif Dastan,
• Haydar Kilic and
• Nurullah Saracoglu

Beilstein J. Org. Chem. 2018, 14, 1120–1180, doi:10.3762/bjoc.14.98

Herpetopanone, a diterpene from Herpetosiphon aurantiacus discovered by isotope labeling

• Xinli Pan,
• Nicole Domin,
• Sebastian Schieferdecker,
• Hirokazu Kage,
• Martin Roth and
• Markus Nett

Beilstein J. Org. Chem. 2017, 13, 2458–2465, doi:10.3762/bjoc.13.242

• configuration, thereby facilitating an intramolecular cyclization to a cyclodeca-1,5-diene by electrophilic attack of the allylic carbocation onto the corresponding double bond. A 1,3-hydride shift by Wagner–Meerwein rearrangement followed by another cyclization would then give rise to an octahydronaphthalene

Synthesis of alkynyl-substituted camphor derivatives and their use in the preparation of paclitaxel-related compounds

• M. Fernanda N. N. Carvalho,
• Rudolf Herrmann and
• Gabriele Wagner

Beilstein J. Org. Chem. 2017, 13, 1230–1238, doi:10.3762/bjoc.13.122

• ], occasionally accompanied by a Wagner–Meerwein rearrangement [23]. However, no such products were found with any of the diynes 4. Our first attempts to employ 4a as a ligand with Ti(IV) resulted, somewhat surprisingly, in the addition of HCl under simultaneous annulation (three-carbon expansion [24][25]) of a

A detailed view on 1,8-cineol biosynthesis by Streptomyces clavuligerus

• Jan Rinkel,
• Patrick Rabe,
• Laura zur Horst and
• Jeroen S. Dickschat

Beilstein J. Org. Chem. 2016, 12, 2317–2324, doi:10.3762/bjoc.12.225

• : Wagner-Meerwein rearrangement. Supporting Information Synthesis schemes, Mosher ester analysis of (R)- and (S)-(1-2H)GPP, gas chromatogram of the enzyme product of 1,8-cineol synthase, 13C NMR of the enzyme product from (2-13C)GPP in deuterium oxide buffer, and full NMR data of 1. Supporting Information

Recent highlights in biosynthesis research using stable isotopes

• Jan Rinkel and
• Jeroen S. Dickschat

Beilstein J. Org. Chem. 2015, 11, 2493–2508, doi:10.3762/bjoc.11.271

• attack of water gives the neutral intermediate germacrene D-4-ol (39). Reprotonation induces the formation of the bicyclic system 40, which can rearrange via two sequential 1,2-hydride shifts to the cation 41. The attack of the hydroxy function and either a 1,2-hydride shift or a Wagner–Meerwein

• rearrangement in a concerted process leads to 42 and 43. The protonation of C-5 was shown by using (2-13C)FPP as a substrate for an in vitro incubation of the terpene synthase in D2O leading to characteristic strongly enhanced triplets for the labeled carbons of 42 and 43 in the 13C NMR spectrum. As an

The chemical behavior of terminally tert-butylated polyolefins

• Dagmar Klein,
• Henning Hopf,
• Peter G. Jones,
• Ina Dix and
• Ralf Hänel

Beilstein J. Org. Chem. 2015, 11, 1246–1258, doi:10.3762/bjoc.11.139

• group is readily seen in the IR spectrum (νmax = 1702 cm−1) and the carbonyl carbon signal in the 13C NMR spectrum at δ = 217 ppm is also of particular diagnostic value. We propose that 31 is produced from epoxide 29 by initial protonation to the oxonium ion 30, which then undergoes a Wagner–Meerwein

• rearrangement followed by deprotonation. Under non-acidic conditions, this process would not be expected; and indeed, when 7 was oxidized with dimethyldioxirane (DMDO) in acetone at room temperature, epoxide 32 with a central oxirane ring is produced in acceptable yield (59%). Since we were unable to obtain

C–H-Functionalization logic guides the synthesis of a carbacyclopamine analog

• Sebastian Rabe,
• Johann Moschner,
• Marina Bantzi,
• Philipp Heretsch and
• Athanassios Giannis

Beilstein J. Org. Chem. 2014, 10, 1564–1569, doi:10.3762/bjoc.10.161

• intermediate in the synthesis of 2 (see Scheme 1). We envisioned a rhodium-catalyzed C–H-insertion into the C17–H bond to occur with a high degree of selectivity (both regio- and stereoselectivity) to form the all-carbon E-ring (for its structure see 11, Scheme 2). Furthermore, a Wagner–Meerwein rearrangement

The chemistry of isoindole natural products

• Klaus Speck and
• Thomas Magauer

Beilstein J. Org. Chem. 2013, 9, 2048–2078, doi:10.3762/bjoc.9.243

• ). After loss of the pyrophosphate group and double cyclization, a 1,3-hydride shift and Wagner–Meerwein rearrangement leads to the naturally occurring ent-atisir-16-ene (231). Oxidative incorporation of nitrogen, which might be derived from β-aminoethanol, generates the atisine-type skeleton 232

Organocatalyzed enantioselective desymmetrization of aziridines and epoxides

• Ping-An Wang

Beilstein J. Org. Chem. 2013, 9, 1677–1695, doi:10.3762/bjoc.9.192

• 90% ee by a Wagner–Meerwein rearrangement. The mechanism of the enantioselective desymmetrization of meso-epoxides by chiral pyridine N-oxides is not fully understood at the time of this writing. Conclusion In this review, we summarized the recent advances of the organocatalyzed enantioselective

Synthesis and Diels–Alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers

• Bilal Nişancı,
• Erdin Dalkılıç,
• Murat Güney and
• Arif Daştan

Beilstein J. Org. Chem. 2009, 5, No. 39, doi:10.3762/bjoc.5.39

• compounds are of great scientific interest because of their unusual geometry and high reactivity. For example, these compounds exhibit a unique behavior in the cationic Wagner–Meerwein rearrangement [1][2][3][4][5][6][7][8][9][10], in the solvolytic reactivity [11], in the photochemical di-π-methane