Catalytic enantioselective diels-alder addition to furan provides a direct synthetic route to many chiral natural products

E. J. Corey; Teck Peng Loh

doi:10.1016/S0040-4039(00)60594-4

Catalytic enantioselective diels-alder addition to furan provides a direct synthetic route to many chiral natural products

E. J. Corey, Teck Peng Loh

Harvard University

科研成果: 期刊稿件 › 文章 › 同行评审

158 引用（Scopus）

摘要

An oxazaborolidine derived from N-tosyl (αS,βR)-β-methyltryptophan (1)catalyzes the Diels-Alder reaction of 2-bromoacrolein and furan with 96:4 enantioselectivity, leading to an efficient synthesis of numerous chiral 7-oxabicyclo[2.2.1]heptene derivatives.

源语言	英语
页（从-至）	3979-3982
页数	4
期刊	Tetrahedron Letters
卷	34
期	25
DOI	https://doi.org/10.1016/S0040-4039(00)60594-4
出版状态	已出版 - 18 6月 1993
已对外发布	是

访问文件

10.1016/S0040-4039(00)60594-4

其它文件与链接

链接到 Scopus 的出版物

引用此

@article{bbc8043db1ed4d10a86989ff953e85d6,

title = "Catalytic enantioselective diels-alder addition to furan provides a direct synthetic route to many chiral natural products",

abstract = "An oxazaborolidine derived from N-tosyl (αS,βR)-β-methyltryptophan (1)catalyzes the Diels-Alder reaction of 2-bromoacrolein and furan with 96:4 enantioselectivity, leading to an efficient synthesis of numerous chiral 7-oxabicyclo[2.2.1]heptene derivatives.",

author = "Corey, {E. J.} and Loh, {Teck Peng}",

year = "1993",

month = jun,

day = "18",

doi = "10.1016/S0040-4039(00)60594-4",

language = "英语",

volume = "34",

pages = "3979--3982",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "25",

}

TY - JOUR

T1 - Catalytic enantioselective diels-alder addition to furan provides a direct synthetic route to many chiral natural products

AU - Corey, E. J.

AU - Loh, Teck Peng

PY - 1993/6/18

Y1 - 1993/6/18

N2 - An oxazaborolidine derived from N-tosyl (αS,βR)-β-methyltryptophan (1)catalyzes the Diels-Alder reaction of 2-bromoacrolein and furan with 96:4 enantioselectivity, leading to an efficient synthesis of numerous chiral 7-oxabicyclo[2.2.1]heptene derivatives.

AB - An oxazaborolidine derived from N-tosyl (αS,βR)-β-methyltryptophan (1)catalyzes the Diels-Alder reaction of 2-bromoacrolein and furan with 96:4 enantioselectivity, leading to an efficient synthesis of numerous chiral 7-oxabicyclo[2.2.1]heptene derivatives.

UR - http://www.scopus.com/inward/record.url?scp=0027160174&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)60594-4

DO - 10.1016/S0040-4039(00)60594-4

M3 - 文章

AN - SCOPUS:0027160174

SN - 0040-4039

VL - 34

SP - 3979

EP - 3982

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 25

ER -

Catalytic enantioselective diels-alder addition to furan provides a direct synthetic route to many chiral natural products

摘要

访问文件

其它文件与链接

指纹

引用此