Literature DB >> 18646772

Use of enantiomerically pure 7-azabicyclo[2.2.1]heptan-2-ol as a chiral template for the synthesis of aminocyclitols.

Ganesh Pandey1, Keshri Nath Tiwari, V G Puranik.   

Abstract

Using enantiopure 7-azabicyclo[2.2.1]heptane-2-ol, the synthesis of cis- as well as trans-2-aminocyclohexanols, dihydroconduramine E-1, and ent-conduramine F-1 has been described.

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Year:  2008        PMID： 18646772     DOI： 10.1021/ol801381t

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


  2 in total

1.  Regio- and stereoselective synthesis of new diaminocyclopentanols.

Authors:  Evgeni A Larin; Valeri S Kochubei; Yuri M Atroshchenko
Journal:  Beilstein J Org Chem       Date:  2014-10-28       Impact factor: 2.883

2.  Regioselectivity in the ring opening of epoxides for the synthesis of aminocyclitols from D-(-)-quinic acid.

Authors:  Tzenge-Lien Shih; Shu-Yu Yang
Journal:  Molecules       Date:  2012-04-16       Impact factor: 4.411
  2 in total

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