An Asymmetric Synthesis of the γ-Amino-β-hydroxy Acid Segment of Hapalosin

Soumyaditya      Mula; Subrata      Chattopadhyay

doi:10.2174/157017806774964468

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

« Previous Next »

Rights & Permissions Print Cite

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.

Export Options

Export File:

RIS (for EndNote, Reference Manager, ProCite)

BibTeX

Text

Content:

Citation Only

Citation and Abstract

About this article

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