Literature DB >> 12520139

Synthesis of aminocyclohexitol via carbon-carbon bond-forming radical cyclization of oxime ether.

Hideto Miyabe1, Akiyoshi Nishiki, Takeaki Naito.   

Abstract

The stannyl radical mediated-cyclization of oxime ether, derived from D-glucose, gave the aminocyclohexitol derivative. Stereoselective C-C bond forming cyclization proceeded via favorable conformers minimizing A(1,3)-strain between the oxime ether group and alpha-substituents.

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Year:  2003        PMID: 12520139     DOI: 10.1248/cpb.51.100

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  1 in total

1.  Synthesis of a new class of aminocyclitol analogues with the conduramine D-2 configuration.

Authors:  Latif Kelebekli; Yunus Kara; Murat Celik
Journal:  Beilstein J Org Chem       Date:  2010-02-15       Impact factor: 2.883

  1 in total

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