Synthesis and Diels-Alder reactions of α,β-unsaturated γ-sultone

Albert W.M. Lee; W. H. Chan; L. S. Jiang; K. W. Poon

doi:10.1039/a700656j

Synthesis and Diels-Alder reactions of α,β-unsaturated γ-sultone

Albert W.M. Lee^*
, W. H. Chan
, L. S. Jiang
, K. W. Poon

^*Corresponding author for this work

Department of Chemistry

Research output: Contribution to journal › Journal article › peer-review

29 Citations (Scopus)

Abstract

An efficient synthesis of prop-1-ene 1,3-sultone 1 and its Diels-Alder reactions are reported; ring-opening reactions of the cycloadducts with nucleophiles and transformations to the sultams were also investigated.

Original language	English
Pages (from-to)	611-612
Number of pages	2
Journal	Chemical Communications
Issue number	6
DOIs	https://doi.org/10.1039/a700656j
Publication status	Published - 1997

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@article{5072d2fcccec47a1a8a41ccc93dec090,

title = "Synthesis and Diels-Alder reactions of α,β-unsaturated γ-sultone",

abstract = "An efficient synthesis of prop-1-ene 1,3-sultone 1 and its Diels-Alder reactions are reported; ring-opening reactions of the cycloadducts with nucleophiles and transformations to the sultams were also investigated.",

author = "Lee, \{Albert W.M.\} and Chan, \{W. H.\} and Jiang, \{L. S.\} and Poon, \{K. W.\}",

year = "1997",

doi = "10.1039/a700656j",

language = "English",

pages = "611--612",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "6",

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TY - JOUR

T1 - Synthesis and Diels-Alder reactions of α,β-unsaturated γ-sultone

AU - Lee, Albert W.M.

AU - Chan, W. H.

AU - Jiang, L. S.

AU - Poon, K. W.

PY - 1997

Y1 - 1997

N2 - An efficient synthesis of prop-1-ene 1,3-sultone 1 and its Diels-Alder reactions are reported; ring-opening reactions of the cycloadducts with nucleophiles and transformations to the sultams were also investigated.

AB - An efficient synthesis of prop-1-ene 1,3-sultone 1 and its Diels-Alder reactions are reported; ring-opening reactions of the cycloadducts with nucleophiles and transformations to the sultams were also investigated.

UR - https://www.scopus.com/pages/publications/0001353068

U2 - 10.1039/a700656j

DO - 10.1039/a700656j

M3 - Journal article

AN - SCOPUS:0001353068

SN - 1359-7345

SP - 611

EP - 612

JO - Chemical Communications

JF - Chemical Communications

IS - 6

ER -

Synthesis and Diels-Alder reactions of α,β-unsaturated γ-sultone

Abstract

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