Literature DB >> 12556169

Total synthesis of (+)-benzastatin E via diastereoselective Grignard addition to 2-acylindoline.

Narihiro Toda1, Mayuko Ori, Kazuko Takami, Keiko Tago, Hiroshi Kogen.   

Abstract

[reaction: see text] A stereoselective total synthesis of (+)-benzastatin E (1) is described. The synthesis involves a diastereoselective Grignard addition to 2-acylindoline 2, which is derived from commercially available (S)-2-indolinecarboxylic acid (3). The unknown absolute configuration of (+)-1 is determined as (9S,10R).

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Year:  2003        PMID: 12556169     DOI: 10.1021/ol027215t

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

Review 1.  Bacterial terpenome.

Authors:  Jeffrey D Rudolf; Tyler A Alsup; Baofu Xu; Zining Li
Journal:  Nat Prod Rep       Date:  2021-05-26       Impact factor: 15.111

2.  Efficient preparation of α-ketoacetals.

Authors:  Francisco Ayala-Mata; Citlalli Barrera-Mendoza; Hugo A Jiménez-Vázquez; Elena Vargas-Díaz; L Gerardo Zepeda
Journal:  Molecules       Date:  2012-11-22       Impact factor: 4.411

  2 in total

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