Publication:
Destannylative Pummerer-type rearrangement of 1-(tributylstannyl)-1-(phenylsulfinyl)- cyclopropane and -ethene.

1

Issued Date

1993-07-23

Resource Type

Article

ISSN

00404020

DOI

10.1016/S0040-4020(01)81835-4

Other identifier(s)

2-s2.0-0027169362

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Tetrahedron. Vol.49, No.30 (1993), 6651-6660

Suggested Citation

Manat Pohmakotr, Srisamorn Sithikanchanakul, Sujitra Khosavanna Destannylative Pummerer-type rearrangement of 1-(tributylstannyl)-1-(phenylsulfinyl)- cyclopropane and -ethene.. Tetrahedron. Vol.49, No.30 (1993), 6651-6660. doi:10.1016/S0040-4020(01)81835-4 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/22533

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Title

Destannylative Pummerer-type rearrangement of 1-(tributylstannyl)-1-(phenylsulfinyl)- cyclopropane and -ethene.

Author(s)

Manat Pohmakotr
 Srisamorn Sithikanchanakul
 Sujitra Khosavanna

Other Contributor(s)

Mahidol University

Abstract

1-(Tributylstannyl)-1-(phenylsulfinyl)-cyclopropane and -ethene were found to react with acyl chlorides to provide the corresponding 1-acyloxy-1-(phenylthio)-cyclopropanes and -ethenes. The reaction involves the Pummerer-type rearrangement with loss of the tributylstannyl group. © 1993.

Keyword(s)

Biochemistry, Genetics and Molecular Biology
 Chemistry
 Pharmacology, Toxicology and Pharmaceutics

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URI

https://repository.li.mahidol.ac.th/handle/123456789/22533

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Scopus 1991-2000