Diels-alder reactions of 2H-thiopyrans

Dale E. Ward; Wajdi M. Zoghaib; Chung K. Rhee; Gai Yuanzhu

doi:10.1016/S0040-4039(00)94643-4

Diels-alder reactions of 2H-thiopyrans

Dale E. Ward^*, Wajdi M. Zoghaib, Chung K. Rhee, Gai Yuanzhu

^*Corresponding author for this work

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

16 Citations (Scopus)

Abstract

Oxygenated 2H-thiopyrans react with typical dienophiles to produce predominantly endo adducts in modest to high yield. The adducts can be desulfurized to give compounds equivalent to a Diels-Alder adduct of a cis -diene.

Original language	English
Pages (from-to)	845-848
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	6
DOIs	https://doi.org/10.1016/S0040-4039(00)94643-4
Publication status	Published - 1990
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)94643-4

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title = "Diels-alder reactions of 2H-thiopyrans",

abstract = "Oxygenated 2H-thiopyrans react with typical dienophiles to produce predominantly endo adducts in modest to high yield. The adducts can be desulfurized to give compounds equivalent to a Diels-Alder adduct of a cis -diene.",

author = "Ward, {Dale E.} and Zoghaib, {Wajdi M.} and Rhee, {Chung K.} and Gai Yuanzhu",

note = "Funding Information: Acknowledgement: Financial support from the Natural Sciences and Engineering Research Council (Canada) and the University of Saskatchewan is gratefully acknowledged.",

year = "1990",

doi = "10.1016/S0040-4039(00)94643-4",

language = "English",

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journal = "Tetrahedron Letters",

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T1 - Diels-alder reactions of 2H-thiopyrans

AU - Ward, Dale E.

AU - Zoghaib, Wajdi M.

AU - Rhee, Chung K.

AU - Yuanzhu, Gai

N1 - Funding Information: Acknowledgement: Financial support from the Natural Sciences and Engineering Research Council (Canada) and the University of Saskatchewan is gratefully acknowledged.

PY - 1990

Y1 - 1990

N2 - Oxygenated 2H-thiopyrans react with typical dienophiles to produce predominantly endo adducts in modest to high yield. The adducts can be desulfurized to give compounds equivalent to a Diels-Alder adduct of a cis -diene.

AB - Oxygenated 2H-thiopyrans react with typical dienophiles to produce predominantly endo adducts in modest to high yield. The adducts can be desulfurized to give compounds equivalent to a Diels-Alder adduct of a cis -diene.

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U2 - 10.1016/S0040-4039(00)94643-4

DO - 10.1016/S0040-4039(00)94643-4

M3 - Article

AN - SCOPUS:0025058929

SN - 0040-4039

VL - 31

SP - 845

EP - 848

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 6

ER -

Diels-alder reactions of 2H-thiopyrans

Abstract

ASJC Scopus subject areas

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