Literature DB >> 15816760

Synthesis of a C20-C26 segment of superstolide A by addition of a chiral allenylzinc reagent to (R)-N-boc alaninal.

James A Marshall1, James J Mulhearn.   

Abstract

[reaction: see text] Additions of chiral allenylzinc and indium reagents to N-Boc alaninal were examined as a possible route to a C20-C26 segment of superstolide A. Allenylzinc reagents, prepared in situ by palladiozincation of (R)- and (S)-5-pivalyloxy-3-butyn-2-ol mesylate, showed excellent reagent control to afford the anti,syn and anti,anti diastereomers as the nearly exclusive adducts.

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Year:  2005        PMID: 15816760     DOI: 10.1021/ol050289v

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


  2 in total

1.  Total synthesis of (+)-superstolide A.

Authors:  Mariola Tortosa; Neal A Yakelis; William R Roush
Journal:  J Org Chem       Date:  2008-12-19       Impact factor: 4.354

2.  Design, synthesis, and biological evaluation of truncated superstolide A.

Authors:  Lei Chen; Kausar Begam Riaz Ahmed; Peng Huang; Zhendong Jin
Journal:  Angew Chem Int Ed Engl       Date:  2013-02-13       Impact factor: 15.336

  2 in total

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