Literature DB >> 11672287

Temporary Silicon-Tethered Ring-Closing Metathesis Approach to C(2)-Symmetrical 1,4-Diols: Asymmetric Synthesis of D-Altritol.

P. Andrew Evans1, V. Srinivasa Murthy.   

Abstract

Entities:  

Year:  1998        PMID： 11672287     DOI： 10.1021/jo9811524

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


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  3 in total

1.  Diastereoselective temporary silicon-tethered ring-closing-metathesis reactions with prochiral alcohols: a new approach to long-range asymmetric induction.

Authors:  P Andrew Evans; Jian Cui; Gerald P Buffone
Journal:  Angew Chem Int Ed Engl       Date:  2003-04-17       Impact factor: 15.336

2.  Enantioselective total synthesis of the potent antitumor agent (-)-mucocin using a temporary silicon-tethered ring-closing metathesis cross-coupling reaction.

Authors:  P Andrew Evans; Jian Cui; Santosh J Gharpure; Alexei Polosukhin; Hai-Ren Zhang
Journal:  J Am Chem Soc       Date:  2003-12-03       Impact factor: 15.419

3.  A highly convergent synthesis of the C1-C31 polyol domain of amphidinol 3 featuring a TST-RCM reaction: confirmation of the revised relative stereochemistry.

Authors:  Aleksandr Grisin; P Andrew Evans
Journal:  Chem Sci       Date:  2015-08-06       Impact factor: 9.825
  3 in total

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