Abstract
A facile synthesis of the title compound has been developed starting from the crotylated product of (R)-cyclohexylideneglyceraldehyde (2). The key features of the synthesis were stereochemical control of the crotylation by alteration of reaction conditions, operational simplicity and the use of inexpensive compounds/reagents.
Keywords: Asymmetric synthesis, (R)-cyclohexylideneglyceraldehyde, hapalosin, β-hydroxy acid
Letters in Organic Chemistry
Title: An Asymmetric Synthesis of the β-Hydroxy Acid Segment of Hapalosin (EXPERIMENTAL)
Volume: 3 Issue: 10
Author(s): Anubha Sharma, Siddharth Roy, Dibakar Goswami, Angshuman Chattopadhyay and Subrata Chattopadhyay
Affiliation:
Keywords: Asymmetric synthesis, (R)-cyclohexylideneglyceraldehyde, hapalosin, β-hydroxy acid
Abstract: A facile synthesis of the title compound has been developed starting from the crotylated product of (R)-cyclohexylideneglyceraldehyde (2). The key features of the synthesis were stereochemical control of the crotylation by alteration of reaction conditions, operational simplicity and the use of inexpensive compounds/reagents.
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Cite this article as:
Sharma Anubha, Roy Siddharth, Goswami Dibakar, Chattopadhyay Angshuman and Chattopadhyay Subrata, An Asymmetric Synthesis of the β-Hydroxy Acid Segment of Hapalosin (EXPERIMENTAL), Letters in Organic Chemistry 2006; 3 (10) . https://dx.doi.org/10.2174/157017806779025997
DOI https://dx.doi.org/10.2174/157017806779025997 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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