Literature DB >> 26833878

Stereoselective Halogenation in Natural Product Synthesis.

Won-jin Chung1, Christopher D Vanderwal2.   

Abstract

At last count, nearly 5000 halogenated natural products have been discovered. In approximately half of these compounds, the carbon atom to which the halogen is bound is sp(3) -hybridized; therefore, there are an enormous number of natural products for which stereocontrolled halogenation must be a critical component of any synthesis strategy. In this Review, we critically discuss the methods and strategies used for stereoselective introduction of halogen atoms in the context of natural product synthesis. Using the successes of the past, we also attempt to identify gaps in our synthesis technology that would aid the synthesis of halogenated natural products, as well as existing methods that have not yet seen application in complex molecule synthesis. The chemistry described herein demonstrates yet again how natural products continue to provide the inspiration for critical advances in chemical synthesis.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  asymmetric synthesis; halogenation; natural products; stereochemistry; total synthesis

Mesh:

Substances:

Year:  2016        PMID: 26833878      PMCID: PMC6028003          DOI: 10.1002/anie.201506388

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  151 in total

Review 1.  New catalytic approaches towards the enantioselective halogenation of alkenes.

Authors:  Ulrich Hennecke
Journal:  Chem Asian J       Date:  2012-02-07

2.  A concise and stereoselective synthesis of hydroxypyrrolidines: rapid synthesis of (+)-preussin.

Authors:  Jason A Draper; Robert Britton
Journal:  Org Lett       Date:  2010-09-17       Impact factor: 6.005

3.  First total synthesis and structural reassignment of (-)-aplysiallene.

Authors:  Jian Wang; Brian L Pagenkopf
Journal:  Org Lett       Date:  2007-08-11       Impact factor: 6.005

Review 4.  Asymmetric enamine catalysis.

Authors:  Santanu Mukherjee; Jung Woon Yang; Sebastian Hoffmann; Benjamin List
Journal:  Chem Rev       Date:  2007-12       Impact factor: 60.622

5.  Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates.

Authors:  Andrej Shemet; David Sarlah; Erick M Carreira
Journal:  Org Lett       Date:  2015-03-26       Impact factor: 6.005

6.  Total synthesis and structural revision of laurefurenynes A and B.

Authors:  Michael T Holmes; Robert Britton
Journal:  Chemistry       Date:  2013-08-19       Impact factor: 5.236

Review 7.  Halogen bonding for rational drug design and new drug discovery.

Authors:  Yunxiang Lu; Yingtao Liu; Zhijian Xu; Haiying Li; Honglai Liu; Weiliang Zhu
Journal:  Expert Opin Drug Discov       Date:  2012-03-30       Impact factor: 6.098

8.  Enantioselective bromolactonization of conjugated (Z)-enynes.

Authors:  Wei Zhang; Suqing Zheng; Na Liu; Jenny B Werness; Ilia A Guzei; Weiping Tang
Journal:  J Am Chem Soc       Date:  2010-03-24       Impact factor: 15.419

9.  Design and synthesis of chiral N-chloroimidodicarbonates: application to asymmetric chlorination of silyl enol ethers.

Authors:  Saumen Hajra; Manishabrata Bhowmick; Biswajit Maji; Debarshi Sinha
Journal:  J Org Chem       Date:  2007-06-02       Impact factor: 4.354

10.  Direct synthesis of imino-C-nucleoside analogues and other biologically active iminosugars.

Authors:  Milan Bergeron-Brlek; Michael Meanwell; Robert Britton
Journal:  Nat Commun       Date:  2015-04-23       Impact factor: 14.919

View more
  32 in total

1.  Function and Structure of MalA/MalA', Iterative Halogenases for Late-Stage C-H Functionalization of Indole Alkaloids.

Authors:  Amy E Fraley; Marc Garcia-Borràs; Ashootosh Tripathi; Dheeraj Khare; Eduardo V Mercado-Marin; Hong Tran; Qingyun Dan; Gabrielle P Webb; Katharine R Watts; Phillip Crews; Richmond Sarpong; Robert M Williams; Janet L Smith; K N Houk; David H Sherman
Journal:  J Am Chem Soc       Date:  2017-08-21       Impact factor: 15.419

2.  Organoselenium-catalyzed enantioselective syn-dichlorination of unbiased alkenes.

Authors:  Bradley B Gilbert; Stanley T-C Eey; Pavel Ryabchuk; Olivia Garry; Scott E Denmark
Journal:  Tetrahedron       Date:  2019-06-01       Impact factor: 2.457

3.  Ketone-catalyzed photochemical C(sp3)-H chlorination.

Authors:  Lei Han; Jibao Xia; Lin You; Chuo Chen
Journal:  Tetrahedron       Date:  2017-05-04       Impact factor: 2.457

4.  Catalytic Enantioselective Addition of an Allyl Group to Ketones Containing a Tri-, a Di-, or a Monohalomethyl Moiety. Stereochemical Control Based on Distinctive Electronic and Steric Attributes of C-Cl, C-Br, and C-F Bonds.

Authors:  Diana C Fager; KyungA Lee; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2019-09-25       Impact factor: 15.419

5.  Catalytic Regio- and Enantioselective Haloazidation of Allylic Alcohols.

Authors:  Frederick J Seidl; Chang Min; Jovan A Lopez; Noah Z Burns
Journal:  J Am Chem Soc       Date:  2018-11-12       Impact factor: 15.419

6.  Catalytic Enantioselective Dihalogenation and the Selective Synthesis of (-)-Deschloromytilipin A and (-)-Danicalipin A.

Authors:  Matthew L Landry; Dennis X Hu; Grace M McKenna; Noah Z Burns
Journal:  J Am Chem Soc       Date:  2016-04-08       Impact factor: 15.419

Review 7.  Enzymatic Halogenation and Dehalogenation Reactions: Pervasive and Mechanistically Diverse.

Authors:  Vinayak Agarwal; Zachary D Miles; Jaclyn M Winter; Alessandra S Eustáquio; Abrahim A El Gamal; Bradley S Moore
Journal:  Chem Rev       Date:  2017-01-20       Impact factor: 60.622

8.  Enantioselective Synthesis of Azamerone.

Authors:  Matthew L Landry; Grace M McKenna; Noah Z Burns
Journal:  J Am Chem Soc       Date:  2019-02-08       Impact factor: 15.419

9.  Kinetically controlled E-selective catalytic olefin metathesis.

Authors:  Thach T Nguyen; Ming Joo Koh; Xiao Shen; Filippo Romiti; Richard R Schrock; Amir H Hoveyda
Journal:  Science       Date:  2016-04-29       Impact factor: 47.728

10.  A Unified Approach for the Enantioselective Synthesis of the Brominated Chamigrene Sesquiterpenes.

Authors:  Alexander J Burckle; Vasil H Vasilev; Noah Z Burns
Journal:  Angew Chem Int Ed Engl       Date:  2016-08-10       Impact factor: 15.336

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.