Abstract
A facile synthesis of the title compound has been developed starting from a homoallylic alcohol that can be conveniently prepared from (R)-cyclohexylidene glyceraldehyde. The key features of the synthesis were its operational simplicity and the use of inexpensive compounds.
Keywords: γ-amino-β-hydroxy acid, asymmetric synthesis, (R)-cyclohexylidene glyceraldehyde, hapalosin
Letters in Organic Chemistry
Title: An Asymmetric Synthesis of the γ-Amino-β-hydroxy Acid Segment of Hapalosin
Volume: 3 Issue: 1
Author(s): Soumyaditya Mula and Subrata Chattopadhyay
Affiliation:
Keywords: γ-amino-β-hydroxy acid, asymmetric synthesis, (R)-cyclohexylidene glyceraldehyde, hapalosin
Abstract: A facile synthesis of the title compound has been developed starting from a homoallylic alcohol that can be conveniently prepared from (R)-cyclohexylidene glyceraldehyde. The key features of the synthesis were its operational simplicity and the use of inexpensive compounds.
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Cite this article as:
Mula Soumyaditya and Chattopadhyay Subrata, An Asymmetric Synthesis of the γ-Amino-β-hydroxy Acid Segment of Hapalosin, Letters in Organic Chemistry 2006; 3 (1) . https://dx.doi.org/10.2174/157017806774964468
DOI https://dx.doi.org/10.2174/157017806774964468 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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