Diastereoselectivity in Michael additions to a pyrrolidinyl enone

Roderick W. Bates; Palangpon Kongsaeree

doi:10.1055/s-1999-2825

Diastereoselectivity in Michael additions to a pyrrolidinyl enone

Roderick W. Bates^*, Palangpon Kongsaeree

^*Corresponding author for this work

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

6 Citations (Scopus)

Abstract

Michael additions of stabilized carabanions to an α-pyrrolidinylenone are highly diastereoselective. Epoxidation is similarly selective.

Original language	English
Pages (from-to)	1307-1309
Number of pages	3
Journal	Synlett
Issue number	8
DOIs	https://doi.org/10.1055/s-1999-2825
Publication status	Published - 1999
Externally published	Yes

ASJC Scopus Subject Areas

Organic Chemistry

Keywords

Diastereoselectivity
Epoxidation
Michael addition

Access to Document

10.1055/s-1999-2825

Cite this

@article{d90896b5ca4e4ae1b970ec9d0c302e38,

title = "Diastereoselectivity in Michael additions to a pyrrolidinyl enone",

abstract = "Michael additions of stabilized carabanions to an α-pyrrolidinylenone are highly diastereoselective. Epoxidation is similarly selective.",

keywords = "Diastereoselectivity, Epoxidation, Michael addition",

author = "Bates, {Roderick W.} and Palangpon Kongsaeree",

year = "1999",

doi = "10.1055/s-1999-2825",

language = "English",

pages = "1307--1309",

journal = "Synlett",

issn = "0936-5214",

publisher = "Georg Thieme Verlag",

number = "8",

}

TY - JOUR

T1 - Diastereoselectivity in Michael additions to a pyrrolidinyl enone

AU - Bates, Roderick W.

AU - Kongsaeree, Palangpon

PY - 1999

Y1 - 1999

N2 - Michael additions of stabilized carabanions to an α-pyrrolidinylenone are highly diastereoselective. Epoxidation is similarly selective.

AB - Michael additions of stabilized carabanions to an α-pyrrolidinylenone are highly diastereoselective. Epoxidation is similarly selective.

KW - Diastereoselectivity

KW - Epoxidation

KW - Michael addition

UR - http://www.scopus.com/inward/record.url?scp=0032806759&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0032806759&partnerID=8YFLogxK

U2 - 10.1055/s-1999-2825

DO - 10.1055/s-1999-2825

M3 - Article

AN - SCOPUS:0032806759

SN - 0936-5214

SP - 1307

EP - 1309

JO - Synlett

JF - Synlett

IS - 8

ER -

Diastereoselectivity in Michael additions to a pyrrolidinyl enone

Abstract

ASJC Scopus Subject Areas

Keywords

Access to Document

Other files and links

Fingerprint

Cite this