Literature DB >> 19255604

High Symmetry Dirhodium(II) Paddlewheel Complexes as Chiral Catalysts.

Jørn Hansen1, Huw M L Davies.   

Abstract

The design and use of chiral dirhodium(II) paddlewheel complexes as catalysts for asymmetric metal carbenoid and metal nitrenoid reactions, and as Lewis acids have become areas of considerable interest during the past two decades. The metal carbenoid chemistry is especially versatile, encompassing transformations such as C-H insertions, cyclopropanations and ylide formation. A number of different classes of dirhodium(II) catalysts have been found to be broadly effective in this chemistry. This review will highlight that many of these catalysts have higher symmetry than the individual chiral ligands themselves. An introduction of theoretical aspects concerning the structure and symmetry of chiral dirhodium(II) complexes will be given followed by an overview of the major classes of catalysts developed to date. Some representative examples of the synthetic potential of these catalysts will also be discussed.

Entities:  

Year:  2008        PMID: 19255604      PMCID: PMC2390838          DOI: 10.1016/j.ccr.2007.08.019

Source DB:  PubMed          Journal:  Coord Chem Rev        ISSN: 0010-8545            Impact factor:   22.315


  30 in total

1.  Recent Advances in Asymmetric Catalytic Metal Carbene Transformations.

Authors:  Michael P. Doyle; David C. Forbes
Journal:  Chem Rev       Date:  1998-04-02       Impact factor: 60.622

2.  Efficient diastereoselective intermolecular rhodium-catalyzed C-H amination.

Authors:  Chungen Liang; Fabien Robert-Peillard; Corinne Fruit; Paul Müller; Robert H Dodd; Philippe Dauban
Journal:  Angew Chem Int Ed Engl       Date:  2006-07-10       Impact factor: 15.336

3.  C-H activation as a strategic reaction: enantioselective synthesis of 4-substituted indoles.

Authors:  Huw M L Davies; James R Manning
Journal:  J Am Chem Soc       Date:  2006-02-01       Impact factor: 15.419

4.  Asymmetric catalytic C-H activation applied to the synthesis of syn-aldol products

Authors: 
Journal:  Org Lett       Date:  2000-12-28       Impact factor: 6.005

5.  Dirhodium tetracarboxylates derived from adamantylglycine as chiral catalysts for enantioselective C-h aminations.

Authors:  Ravisekhara P Reddy; Huw M L Davies
Journal:  Org Lett       Date:  2006-10-26       Impact factor: 6.005

6.  Development of dirhodium(II)-catalyzed generation and enantioselective 1,3-dipolar cycloaddition of carbonyl ylides.

Authors:  D M Hodgson; P A Stupple; F Y Pierard; A H Labande; C Johnstone
Journal:  Chemistry       Date:  2001-10-15       Impact factor: 5.236

7.  Catalytic asymmetric reactions for organic synthesis: the combined C-H activation/siloxy-cope rearrangement.

Authors:  Huw M L Davies; Rohan E J Beckwith
Journal:  J Org Chem       Date:  2004-12-24       Impact factor: 4.354

8.  Discovery of exceptionally efficient catalysts for solvent-free enantioselective hetero-Diels-Alder reaction.

Authors:  Jiang Long; Jieyu Hu; Xiaoqiang Shen; Baoming Ji; Kuiling Ding
Journal:  J Am Chem Soc       Date:  2002-01-09       Impact factor: 15.419

9.  Enantioselective carbon-hydrogen insertion is an effective and efficient methodology for the synthesis of (R)-(-)-baclofen.

Authors:  Michael P Doyle; Wenhao Hu
Journal:  Chirality       Date:  2002 Feb-Mar       Impact factor: 2.437

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

View more
  24 in total

1.  The chiral crown conformation in paddlewheel complexes.

Authors:  Andrew DeAngelis; David T Boruta; Jean-Bernard Lubin; James N Plampin; Glenn P A Yap; Joseph M Fox
Journal:  Chem Commun (Camb)       Date:  2010-05-11       Impact factor: 6.222

2.  Controlling factors for C-H functionalization versus cyclopropanation of dihydronaphthalenes.

Authors:  Etienne Nadeau; Dominic L Ventura; Jonathan A Brekan; Huw M L Davies
Journal:  J Org Chem       Date:  2010-03-19       Impact factor: 4.354

3.  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

4.  Highly enantioselective trapping of zwitterionic intermediates by imines.

Authors:  Huang Qiu; Ming Li; Li-Qin Jiang; Feng-Ping Lv; Li Zan; Chang-Wei Zhai; Michael P Doyle; Wen-Hao Hu
Journal:  Nat Chem       Date:  2012-07-29       Impact factor: 24.427

5.  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

6.  Site-selective and stereoselective functionalization of non-activated tertiary C-H bonds.

Authors:  Kuangbiao Liao; Thomas C Pickel; Vyacheslav Boyarskikh; John Bacsa; Djamaladdin G Musaev; Huw M L Davies
Journal:  Nature       Date:  2017-11-20       Impact factor: 49.962

7.  Reactions of Rh2(CH3COO)4 with thiols and thiolates: a structural study.

Authors:  Alejandra Enriquez Garcia; Farideh Jalilehvand; Pantea Niksirat
Journal:  J Synchrotron Radiat       Date:  2019-02-13       Impact factor: 2.616

8.  Site-selective and stereoselective functionalization of unactivated C-H bonds.

Authors:  Kuangbiao Liao; Solymar Negretti; Djamaladdin G Musaev; John Bacsa; Huw M L Davies
Journal:  Nature       Date:  2016-05-12       Impact factor: 49.962

9.  Rh2(S-biTISP)2-catalyzed asymmetric functionalization of indoles and pyrroles with vinylcarbenoids.

Authors:  Yajing Lian; Huw M L Davies
Journal:  Org Lett       Date:  2012-03-27       Impact factor: 6.005

10.  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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.