Facile enantioselective synthesis of two new bicyclic chiral templates

Kevin D. Belfield; Jeongbeob Seo

doi:10.1080/00397919508011379

Facile enantioselective synthesis of two new bicyclic chiral templates

Kevin D. Belfield, Jeongbeob Seo

Research output: Contribution to journal › Article › peer-review

9 Scopus citations

Abstract

Optically active bicyclic dienes, 4 and 5 have been enantioselectively prepared in three and four steps, respectively. Mixtures of predominantly either the R or S enantiomer were obtained via an asymmetric alkylation of a chiral enamine.

Original language	English (US)
Pages (from-to)	461-466
Number of pages	6
Journal	Synthetic Communications
Volume	25
Issue number	4
DOIs	https://doi.org/10.1080/00397919508011379
State	Published - Feb 1 1995
Externally published	Yes

All Science Journal Classification (ASJC) codes

Organic Chemistry

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10.1080/00397919508011379

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title = "Facile enantioselective synthesis of two new bicyclic chiral templates",

abstract = "Optically active bicyclic dienes, 4 and 5 have been enantioselectively prepared in three and four steps, respectively. Mixtures of predominantly either the R or S enantiomer were obtained via an asymmetric alkylation of a chiral enamine.",

author = "Belfield, \{Kevin D.\} and Jeongbeob Seo",

note = "Funding Information: Acknowledgements. We wish to acknowledge Prof. John E. Baldwin (Syracuse University) for the use of the chiral GC equipment, Dr. Andrew Tyler (Harvard University) for the high-resolution MS, and the University of Detroit Mercy for financial support of this work.",

year = "1995",

month = feb,

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doi = "10.1080/00397919508011379",

language = "English (US)",

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pages = "461--466",

journal = "Synthetic Communications",

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number = "4",

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T1 - Facile enantioselective synthesis of two new bicyclic chiral templates

AU - Belfield, Kevin D.

AU - Seo, Jeongbeob

N1 - Funding Information: Acknowledgements. We wish to acknowledge Prof. John E. Baldwin (Syracuse University) for the use of the chiral GC equipment, Dr. Andrew Tyler (Harvard University) for the high-resolution MS, and the University of Detroit Mercy for financial support of this work.

PY - 1995/2/1

Y1 - 1995/2/1

N2 - Optically active bicyclic dienes, 4 and 5 have been enantioselectively prepared in three and four steps, respectively. Mixtures of predominantly either the R or S enantiomer were obtained via an asymmetric alkylation of a chiral enamine.

AB - Optically active bicyclic dienes, 4 and 5 have been enantioselectively prepared in three and four steps, respectively. Mixtures of predominantly either the R or S enantiomer were obtained via an asymmetric alkylation of a chiral enamine.

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U2 - 10.1080/00397919508011379

DO - 10.1080/00397919508011379

M3 - Article

AN - SCOPUS:0028852425

SN - 0039-7911

VL - 25

SP - 461

EP - 466

JO - Synthetic Communications

JF - Synthetic Communications

IS - 4

ER -

Facile enantioselective synthesis of two new bicyclic chiral templates

Abstract

All Science Journal Classification (ASJC) codes

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