Enantiospecific synthesis of (+)-altholactone and its three stereoisomers

Tony K.M. Shing; John G. Gillhouley

doi:10.1016/S0040-4020(01)85344-8

Enantiospecific synthesis of (+)-altholactone and its three stereoisomers

Tony K.M. Shing, John G. Gillhouley

化学科

研究成果: Article › 査読

32 被引用数 (Scopus)

抄録

(+)-Altholactone 1 and (+)-7-epi-altholactone 3 were constructed from D-gulonolactone whereas their respective enantiomers (-)-altholactone 2 and (-)-7-epi- altholactone 4 were synthesised from D-mannose, involving stereocontrolled reduction of the lactols 21 and 12 as a key step.

本文言語	English
ページ（範囲）	8685-8698
ページ数	14
ジャーナル	Tetrahedron
巻	50
号	29
DOI	https://doi.org/10.1016/S0040-4020(01)85344-8
出版ステータス	Published - 1994

ASJC Scopus subject areas

生化学
創薬
有機化学

文献へのアクセス

10.1016/S0040-4020(01)85344-8

他のファイルとリンク

引用スタイル

@article{bd3158b77bf24a6bb6f612f29083ba76,

title = "Enantiospecific synthesis of (+)-altholactone and its three stereoisomers",

abstract = "(+)-Altholactone 1 and (+)-7-epi-altholactone 3 were constructed from D-gulonolactone whereas their respective enantiomers (-)-altholactone 2 and (-)-7-epi- altholactone 4 were synthesised from D-mannose, involving stereocontrolled reduction of the lactols 21 and 12 as a key step.",

author = "Shing, {Tony K.M.} and Gillhouley, {John G.}",

year = "1994",

doi = "10.1016/S0040-4020(01)85344-8",

language = "English",

volume = "50",

pages = "8685--8698",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier Limited",

number = "29",

}

TY - JOUR

T1 - Enantiospecific synthesis of (+)-altholactone and its three stereoisomers

AU - Shing, Tony K.M.

AU - Gillhouley, John G.

PY - 1994

Y1 - 1994

N2 - (+)-Altholactone 1 and (+)-7-epi-altholactone 3 were constructed from D-gulonolactone whereas their respective enantiomers (-)-altholactone 2 and (-)-7-epi- altholactone 4 were synthesised from D-mannose, involving stereocontrolled reduction of the lactols 21 and 12 as a key step.

AB - (+)-Altholactone 1 and (+)-7-epi-altholactone 3 were constructed from D-gulonolactone whereas their respective enantiomers (-)-altholactone 2 and (-)-7-epi- altholactone 4 were synthesised from D-mannose, involving stereocontrolled reduction of the lactols 21 and 12 as a key step.

UR - http://www.scopus.com/inward/record.url?scp=0027969128&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0027969128&partnerID=8YFLogxK

U2 - 10.1016/S0040-4020(01)85344-8

DO - 10.1016/S0040-4020(01)85344-8

M3 - Article

AN - SCOPUS:0027969128

VL - 50

SP - 8685

EP - 8698

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 29

ER -

Enantiospecific synthesis of (+)-altholactone and its three stereoisomers

抄録

ASJC Scopus subject areas

文献へのアクセス

他のファイルとリンク

フィンガープリント

引用スタイル