Enantioselective synthesis of attenols A and B

Kiyotake Suenaga, Keisuke Araki, Tetsuya Sengoku, Daisuke Uemura

Research output: Contribution to journalArticle

46 Citations (Scopus)

Abstract

(Matrix presented) Enantioselective synthesis of attenols A and B was accomplished by using diastereoselective hydroboration, Lindlar reduction, and acid-catalyzed acetal formation.

Original languageEnglish
Pages (from-to)527-529
Number of pages3
JournalOrganic Letters
Volume3
Issue number4
DOIs
Publication statusPublished - 2001 Feb 22
Externally publishedYes

Fingerprint

hydroboration
acetals
Acetals
acids
synthesis
matrices
Acids
attenol A

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

Enantioselective synthesis of attenols A and B. / Suenaga, Kiyotake; Araki, Keisuke; Sengoku, Tetsuya; Uemura, Daisuke.

In: Organic Letters, Vol. 3, No. 4, 22.02.2001, p. 527-529.

Research output: Contribution to journalArticle

Suenaga, K, Araki, K, Sengoku, T & Uemura, D 2001, 'Enantioselective synthesis of attenols A and B', Organic Letters, vol. 3, no. 4, pp. 527-529. https://doi.org/10.1021/ol006905z
Suenaga, Kiyotake ; Araki, Keisuke ; Sengoku, Tetsuya ; Uemura, Daisuke. / Enantioselective synthesis of attenols A and B. In: Organic Letters. 2001 ; Vol. 3, No. 4. pp. 527-529.
@article{4dd553babc0d40a2945b7fc19cb02083,
title = "Enantioselective synthesis of attenols A and B",
abstract = "(Matrix presented) Enantioselective synthesis of attenols A and B was accomplished by using diastereoselective hydroboration, Lindlar reduction, and acid-catalyzed acetal formation.",
author = "Kiyotake Suenaga and Keisuke Araki and Tetsuya Sengoku and Daisuke Uemura",
year = "2001",
month = "2",
day = "22",
doi = "10.1021/ol006905z",
language = "English",
volume = "3",
pages = "527--529",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "4",

}

TY - JOUR

T1 - Enantioselective synthesis of attenols A and B

AU - Suenaga, Kiyotake

AU - Araki, Keisuke

AU - Sengoku, Tetsuya

AU - Uemura, Daisuke

PY - 2001/2/22

Y1 - 2001/2/22

N2 - (Matrix presented) Enantioselective synthesis of attenols A and B was accomplished by using diastereoselective hydroboration, Lindlar reduction, and acid-catalyzed acetal formation.

AB - (Matrix presented) Enantioselective synthesis of attenols A and B was accomplished by using diastereoselective hydroboration, Lindlar reduction, and acid-catalyzed acetal formation.

UR - http://www.scopus.com/inward/record.url?scp=0035932063&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0035932063&partnerID=8YFLogxK

U2 - 10.1021/ol006905z

DO - 10.1021/ol006905z

M3 - Article

C2 - 11178816

AN - SCOPUS:0035932063

VL - 3

SP - 527

EP - 529

JO - Organic Letters

JF - Organic Letters

SN - 1523-7060

IS - 4

ER -