Literature DB >> 19847341

Application of donor/acceptor-carbenoids to the synthesis of natural products.

Huw M L Davies1, Justin R Denton.   

Abstract

The metal catalyzed reactions of diazo compounds have been broadly used in organic synthesis. The resulting metal-carbenoid intermediates are capable of undergoing a range of unconventional reactions, and due to their high energy, they are ideal for initiating cascade sequences leading to the rapid generation of structural complexity. This tutorial review will give an overview of the most versatile reactions of donor/acceptor carbenoids, an exciting class of intermediates capable of highly selective reactions. This will include cyclopropanation, [4 + 3] cycloaddition, and C-H functionalization methodologies. The application of this chemistry to the synthesis of a range of natural products will be described.

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Year:  2009        PMID: 19847341      PMCID: PMC3397165          DOI: 10.1039/b901170f

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  27 in total

1.  Catalytic and enantioselective allylic C-H activation with donor-acceptor-substituted carbenoids.

Authors:  Huw M L Davies; Joachim Nikolai
Journal:  Org Biomol Chem       Date:  2005-10-31       Impact factor: 3.876

2.  Direct synthesis of (+)-erogorgiaene through a kinetic enantiodifferentiating step.

Authors:  Huw M L Davies; Abbas M Walji
Journal:  Angew Chem Int Ed Engl       Date:  2005-03-04       Impact factor: 15.336

3.  Enantiospecific Sn(II)- and Sn(IV)-catalyzed cycloadditions of aldehydes and donor-acceptor cyclopropanes.

Authors:  Patrick D Pohlhaus; Jeffrey S Johnson
Journal:  J Am Chem Soc       Date:  2005-11-23       Impact factor: 15.419

4.  Total Synthesis of (+/-)-Tremulenolide A and (+/-)-Tremulenediol A via a Stereoselective Cyclopropanation/Cope Rearrangement Annulation Strategy.

Authors:  Huw M. L. Davies; Brian D. Doan
Journal:  J Org Chem       Date:  1998-02-06       Impact factor: 4.354

5.  Enantio- and diastereoselective synthesis of cis-2-aryl-3-methoxycarbonyl-2,3-dihydrobenzofurans via the Rh(II)-catalyzed C-H insertion process.

Authors:  Hiroaki Saito; Hiroyuki Oishi; Shinji Kitagaki; Seiichi Nakamura; Masahiro Anada; Shunichi Hashimoto
Journal:  Org Lett       Date:  2002-10-31       Impact factor: 6.005

6.  Asymmetric [4 + 3] cycloadditions between vinylcarbenoids and dienes: application to the total synthesis of the natural product (-)-5-epi-vibsanin E.

Authors:  Brett D Schwartz; Justin R Denton; Yajing Lian; Huw M L Davies; Craig M Williams
Journal:  J Am Chem Soc       Date:  2009-06-17       Impact factor: 15.419

Review 7.  Catalytic C-H functionalization by metal carbenoid and nitrenoid insertion.

Authors:  Huw M L Davies; James R Manning
Journal:  Nature       Date:  2008-01-24       Impact factor: 49.962

8.  Parallel kinetic resolution approach to the cyathane and cyanthiwigin diterpenes using a cyclopropanation/Cope rearrangement.

Authors:  Laura C Miller; J Maina Ndungu; Richmond Sarpong
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

9.  Synthesis of (-)-hamigeran B.

Authors:  Douglass F Taber; Weiwei Tian
Journal:  J Org Chem       Date:  2008-09-05       Impact factor: 4.354

10.  Catalytic asymmetric reactions for organic synthesis: the combined C-H activation/Cope rearrangement.

Authors:  Huw M L Davies; Qihui Jin
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-15       Impact factor: 11.205

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  46 in total

1.  Electronic structure and bonding of the dinuclear metal M2(CO)10 decacarbonyls: applications of natural orbitals for chemical valence.

Authors:  Rafik Menacer; Abdelghani May; Lotfi Belkhiri; Abdelhamid Mousser
Journal:  J Mol Model       Date:  2017-11-28       Impact factor: 1.810

2.  Combined C-H functionalization/Cope rearrangement with vinyl ethers as a surrogate for the vinylogous Mukaiyama aldol reaction.

Authors:  Yajing Lian; Huw M L Davies
Journal:  J Am Chem Soc       Date:  2011-07-18       Impact factor: 15.419

3.  Computationally guided stereocontrol of the combined C-H functionalization/Cope rearrangement.

Authors:  Yajing Lian; Kenneth I Hardcastle; Huw M L Davies
Journal:  Angew Chem Int Ed Engl       Date:  2011-08-30       Impact factor: 15.336

4.  Divergent Reactivity of Rhodium(I) Carbenes Derived from Indole Annulations.

Authors:  Xiaoxun Li; Hui Li; Wangze Song; Po-Sen Tseng; Lingyan Liu; Ilia A Guzei; Weiping Tang
Journal:  Angew Chem Int Ed Engl       Date:  2015-09-07       Impact factor: 15.336

5.  Stereoselective Cyclopropanation of Electron-Deficient Olefins with a Cofactor Redesigned Carbene Transferase Featuring Radical Reactivity.

Authors:  Daniela M Carminati; Rudi Fasan
Journal:  ACS Catal       Date:  2019-09-05       Impact factor: 13.084

6.  Total Synthesis of (+)-Pancratistatin by the Rh(III)-Catalyzed Addition of a Densely Functionalized Benzamide to a Sugar-Derived Nitroalkene.

Authors:  Tyler J Potter; Jonathan A Ellman
Journal:  Org Lett       Date:  2017-05-24       Impact factor: 6.005

7.  Asymmetric Synthesis of Highly Functionalized Cyclopentanes by a Rhodium- and Scandium-Catalyzed Five-Step Domino Sequence.

Authors:  Brendan T Parr; Zhanjie Li; Huw M L Davies
Journal:  Chem Sci       Date:  2011-09-02       Impact factor: 9.825

8.  Rhodium-catalyzed ring expansion of cyclopropanes to seven-membered rings by 1,5 C-C bond migration.

Authors:  Xiaoxun Li; Min Zhang; Dongxu Shu; Patrick J Robichaux; Suyu Huang; Weiping Tang
Journal:  Angew Chem Int Ed Engl       Date:  2011-09-09       Impact factor: 15.336

9.  Expanding the family of heterobimetallic Bi-Rh paddlewheel carboxylate complexes via equatorial carboxylate exchange.

Authors:  Travis L Sunderland; John F Berry
Journal:  Dalton Trans       Date:  2016-01-07       Impact factor: 4.390

10.  Generation of rhodium(I) carbenes from ynamides and their reactions with alkynes and alkenes.

Authors:  Renhe Liu; Gabrielle N Winston-McPherson; Zhong-Yue Yang; Xin Zhou; Wangze Song; Ilia A Guzei; Xiufang Xu; Weiping Tang
Journal:  J Am Chem Soc       Date:  2013-05-23       Impact factor: 15.419

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