Enantioselective synthesis of attenols A and B

K Suenaga; K Araki; T Sengoku; D Uemura

doi:10.1021/ol006905z

Enantioselective synthesis of attenols A and B

Org Lett. 2001 Feb 22;3(4):527-9. doi: 10.1021/ol006905z.

Authors

K Suenaga¹, K Araki, T Sengoku, D Uemura

Affiliation

¹ Department of Chemistry, Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan. uemura@chem3.chem.nagoya-u.ac.jp

PMID: 11178816
DOI: 10.1021/ol006905z

Abstract

[reaction: see text] Enantioselective synthesis of attenols A and B was accomplished by using diastereoselective hydroboration, Lindlar reduction, and acid-catalyzed acetal formation.

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Animals
Bivalvia
Ethers, Cyclic / chemical synthesis*
Ethers, Cyclic / chemistry
Molecular Conformation
Molecular Structure
Stereoisomerism
Structure-Activity Relationship

Substances

Ethers, Cyclic
attenol A