A convenient synthesis of chiral nonracemic vinyl aziridines

D. Morton; D. Pearson; R.A. Field; R.A. Stockman

doi:10.1021/ol049252l

A convenient synthesis of chiral nonracemic vinyl aziridines

D. Morton, D. Pearson, R.A. Field, R.A. Stockman

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

Abstract

(Equation Presented). The preparation of a range of alkyl and aryl chiral vinyl aziridines was achieved in high yield and stereoselectivity, and with excellent diastereoselectivity, by reaction of tert-butylsulfinylimines with the ylide derived from S-allyl tetrahydrothiophenium bromide.

Original language	Undefined
Pages (from-to)	2377-2380
Number of pages	4
Journal	Organic Letters
DOIs	https://doi.org/10.1021/ol049252l
Publication status	Published - 2004

Keywords

Aziridines
Rings (components)
Aziridine ring

Research Beacons, Institutes and Platforms

Manchester Institute of Biotechnology

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10.1021/ol049252l

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title = "A convenient synthesis of chiral nonracemic vinyl aziridines",

abstract = "(Equation Presented). The preparation of a range of alkyl and aryl chiral vinyl aziridines was achieved in high yield and stereoselectivity, and with excellent diastereoselectivity, by reaction of tert-butylsulfinylimines with the ylide derived from S-allyl tetrahydrothiophenium bromide.",

keywords = "Aziridines, Rings (components), Aziridine ring",

author = "D. Morton and D. Pearson and R.A. Field and R.A. Stockman",

year = "2004",

doi = "10.1021/ol049252l",

language = "Undefined",

pages = "2377--2380",

journal = "Organic Letters",

issn = "1523-7052",

publisher = "American Chemical Society",

}

TY - JOUR

T1 - A convenient synthesis of chiral nonracemic vinyl aziridines

AU - Morton, D.

AU - Pearson, D.

AU - Field, R.A.

AU - Stockman, R.A.

PY - 2004

Y1 - 2004

N2 - (Equation Presented). The preparation of a range of alkyl and aryl chiral vinyl aziridines was achieved in high yield and stereoselectivity, and with excellent diastereoselectivity, by reaction of tert-butylsulfinylimines with the ylide derived from S-allyl tetrahydrothiophenium bromide.

AB - (Equation Presented). The preparation of a range of alkyl and aryl chiral vinyl aziridines was achieved in high yield and stereoselectivity, and with excellent diastereoselectivity, by reaction of tert-butylsulfinylimines with the ylide derived from S-allyl tetrahydrothiophenium bromide.

KW - Aziridines

KW - Rings (components)

KW - Aziridine ring

UR - http://www.scopus.com/inward/record.url?eid=2-s2.0-3242726231&partnerID=MN8TOARS

UR - https://www.scopus.com/pages/publications/3242726231

U2 - 10.1021/ol049252l

DO - 10.1021/ol049252l

M3 - Article

SN - 1523-7052

SP - 2377

EP - 2380

JO - Organic Letters

JF - Organic Letters

ER -

A convenient synthesis of chiral nonracemic vinyl aziridines

Abstract

Keywords

Research Beacons, Institutes and Platforms

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