This submission belongs to the session a. General Organic Synthesis of the event The 1st International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Sep, 1997
Citation
Elliad R. Silcoff, Tuvia Sheradsky, The Synthesis of (2R,5R)-2-Amino-5-Hydroxyhexanoic Acid by Intermolecular Cycloaddition, in Proceedings of The 1st International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 1997, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-1-02026
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The Synthesis of (2R,5R)-2-Amino-5-Hydroxyhexanoic Acid by Intermolecular Cycloaddition
Tuvia Sheradsky 1
Elliad R. Silcoff 1
1. The Hebrew University Jerusalem, 91904 Israel
Abstract
The enantioselective synthesis of alpha amino acids which contain an additional chiral center at a remote position presents an important and complex synthetic problem. We have previously described the employment of a hetero Diels-Alder reaction for this purpose.1 In this project this methodology was notably extended, as demonstrated by the short synthesis of (2R,5R)-2-amino-4-hydroxyhexanoic acid.
Keywords
n/a
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