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Highly regioselective ring-opening of trisubstituted aziridines by sulfur-stabilised carbanions

journal contribution
posted on 2023-05-17, 07:52 authored by Carballares, S, Craig, D, Hyland, CJT, Lu, P, Mathie, T, White, AJP
The highly regioselective, stereospecific ring-opening of trisubstituted N-tosylaziridines possessing vinyl and hydroxymethyl groups by sulfone-and sulfide-stablised carbanions is reported.

History

Publication title

Chemical Communications

Volume

2009

Issue

4

Pagination

451-453

ISSN

1359-7345

Department/School

School of Natural Sciences

Publisher

Royal Soc Chemistry

Place of publication

Thomas Graham House, Science Park, Milton Rd, Cambridge, England, Cambs, Cb4 0Wf

Repository Status

  • Restricted

Socio-economic Objectives

Expanding knowledge in the chemical sciences

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    University Of Tasmania

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