Gold(I)-catalysed synthesis of cyclic sulfamidates by intramolecular allene hydroamination

Mari Higginbotham; Magnus William Paul Bebbington

doi:10.1039/C2CC33711H

Gold(I)-catalysed synthesis of cyclic sulfamidates by intramolecular allene hydroamination

Mari Higginbotham
, Magnus William Paul Bebbington

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

26 Citations (Scopus)

Abstract

Six-membered cyclic sulfamidates are prepared in high yields by treatment of allenic sulfamates with readily available gold(I) complexes. The reaction enable formation of N-substituted quaternary centres and complements existing methods for sulfamidate formation.

Original language	English
Pages (from-to)	7565-7567
Number of pages	3
Journal	Chemical Communications
Volume	48
Issue number	61
DOIs	https://doi.org/10.1039/C2CC33711H
Publication status	Published - 7 Aug 2012

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title = "Gold(I)-catalysed synthesis of cyclic sulfamidates by intramolecular allene hydroamination",

abstract = "Six-membered cyclic sulfamidates are prepared in high yields by treatment of allenic sulfamates with readily available gold(I) complexes. The reaction enable formation of N-substituted quaternary centres and complements existing methods for sulfamidate formation.",

author = "Mari Higginbotham and Bebbington, \{Magnus William Paul\}",

year = "2012",

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day = "7",

doi = "10.1039/C2CC33711H",

language = "English",

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journal = "Chemical Communications",

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publisher = "Royal Society of Chemistry",

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AU - Higginbotham, Mari

AU - Bebbington, Magnus William Paul

PY - 2012/8/7

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N2 - Six-membered cyclic sulfamidates are prepared in high yields by treatment of allenic sulfamates with readily available gold(I) complexes. The reaction enable formation of N-substituted quaternary centres and complements existing methods for sulfamidate formation.

AB - Six-membered cyclic sulfamidates are prepared in high yields by treatment of allenic sulfamates with readily available gold(I) complexes. The reaction enable formation of N-substituted quaternary centres and complements existing methods for sulfamidate formation.

U2 - 10.1039/C2CC33711H

DO - 10.1039/C2CC33711H

M3 - Article

AN - SCOPUS:84863691721

SN - 1359-7345

VL - 48

SP - 7565

EP - 7567

JO - Chemical Communications

JF - Chemical Communications

IS - 61

ER -

Gold(I)-catalysed synthesis of cyclic sulfamidates by intramolecular allene hydroamination

Abstract

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