Literature DB >> 17492815

Substrate-controlled asymmetric total synthesis of (+)-microcladallene B with a bromination strategy based on a nucleophile-assisting leaving group.

Janghyun Park1, Byungsook Kim, Hyoungsu Kim, Sanghee Kim, Deukjoon Kim.   

Abstract

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Year:  2007        PMID： 17492815     DOI： 10.1002/anie.200700854

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


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  4 in total

1.  Diastereoselective, Zinc-Catalyzed Alkynylation of α-Bromo Oxocarbenium Ions.

Authors:  Tatsiana Haidzinskaya; Hilary A Kerchner; Jixin Liu; Mary P Watson
Journal:  Org Lett       Date:  2015-07-21       Impact factor: 6.005

2.  Nucleophile assisting leaving groups: a strategy for aliphatic 18F-fluorination.

Authors:  Shuiyu Lu; Salvatore D Lepore; Song Ye Li; Deboprosad Mondal; Pamela C Cohn; Anjan K Bhunia; Victor W Pike
Journal:  J Org Chem       Date:  2009-08-07       Impact factor: 4.354

3.  Allylic and allenic halide synthesis via NbCl(5)- and NbBr(5)-mediated alkoxide rearrangements.

Authors:  P C Ravikumar; Lihua Yao; Fraser F Fleming
Journal:  J Org Chem       Date:  2009-10-02       Impact factor: 4.354

Review 4.  Stereoselective Halogenation in Natural Product Synthesis.

Authors:  Won-jin Chung; Christopher D Vanderwal
Journal:  Angew Chem Int Ed Engl       Date:  2016-02-02       Impact factor: 15.336
  4 in total

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