Reactions of carbenes bearing sulphide linkages at the δ-position

Kiyosi Kondo; Iwao Ojima

doi:10.1039/C39720000860

Reactions of carbenes bearing sulphide linkages at the δ-position

Kiyosi Kondo
, Iwao Ojima

Chemistry

Sagami Chemical Research Institute

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

25 Scopus citations

Abstract

The carbenes generated from γ-allylthiobutyrophenone tosylhydrazone and carbenoids from 4-benzyl- and 4-allyl-thio-1-diazobutan-2-one give thiolan and thiolanone derivatives, respectively, via cyclic sulphonium ylide intermediates.

Original language	English
Pages (from-to)	860-861
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Volume	0
Issue number	15
DOIs	https://doi.org/10.1039/C39720000860
State	Published - 1972

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abstract = "The carbenes generated from γ-allylthiobutyrophenone tosylhydrazone and carbenoids from 4-benzyl- and 4-allyl-thio-1-diazobutan-2-one give thiolan and thiolanone derivatives, respectively, via cyclic sulphonium ylide intermediates.",

author = "Kiyosi Kondo and Iwao Ojima",

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AU - Ojima, Iwao

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AB - The carbenes generated from γ-allylthiobutyrophenone tosylhydrazone and carbenoids from 4-benzyl- and 4-allyl-thio-1-diazobutan-2-one give thiolan and thiolanone derivatives, respectively, via cyclic sulphonium ylide intermediates.

UR - https://www.scopus.com/pages/publications/37049121342

U2 - 10.1039/C39720000860

DO - 10.1039/C39720000860

M3 - Article

AN - SCOPUS:37049121342

SN - 0022-4936

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EP - 861

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 15

ER -

Reactions of carbenes bearing sulphide linkages at the δ-position

Abstract

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