Use of Enantiomerically Pure 7-Azabicyclo[2.2.1]heptan-2-ol as a Chiral Template for the Synthesis of Aminocyclitols

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.

Saved in:
Bibliographic Details
Published in:Organic letters 2008-08, Vol.10 (16), p.3611-3614
Main Authors: Pandey, Ganesh, Tiwari, Keshri Nath, Puranik, V. G
Format: Article
Language:English
Subjects:
Amines - chemical synthesis
Amines - chemistry
Azabicyclo Compounds - chemistry
Crystallography, X-Ray
Cyclitols - chemical synthesis
Cyclitols - chemistry
Models, Molecular
Molecular Conformation
Stereoisomerism
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary: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.
ISSN:1523-7060
1523-7052
DOI:10.1021/ol801381t