A facile synthesis of 4-arylbutyrolactones via the palladium-catalyzed arylation of 1,3-dioxep-5-ene

Takao Sakamoto; Yoshinori Kondo; Hiroshi Yamanaka

doi:10.3987/COM-93-6499

A facile synthesis of 4-arylbutyrolactones via the palladium-catalyzed arylation of 1,3-dioxep-5-ene

Takao Sakamoto, Yoshinori Kondo, Hiroshi Yamanaka

PHA - Molecular Pharmaceutical Science

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

14 Citations (Scopus)

Abstract

1,3-Dioxep-5-ene was arylated by using Heck reaction, and the arylated 1,3-dioxep-4-ene derivatives were easily converted into 4-arylbutyrolactones, intermediates for the synthesis of natural products and biological active compounds.

Original language	English
Pages (from-to)	2437-2440
Number of pages	4
Journal	Heterocycles
Volume	36
Issue number	11
DOIs	https://doi.org/10.3987/COM-93-6499
Publication status	Published - 1993 Nov 1

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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title = "A facile synthesis of 4-arylbutyrolactones via the palladium-catalyzed arylation of 1,3-dioxep-5-ene",

abstract = "1,3-Dioxep-5-ene was arylated by using Heck reaction, and the arylated 1,3-dioxep-4-ene derivatives were easily converted into 4-arylbutyrolactones, intermediates for the synthesis of natural products and biological active compounds.",

author = "Takao Sakamoto and Yoshinori Kondo and Hiroshi Yamanaka",

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AU - Sakamoto, Takao

AU - Kondo, Yoshinori

AU - Yamanaka, Hiroshi

PY - 1993/11/1

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ER -

A facile synthesis of 4-arylbutyrolactones via the palladium-catalyzed arylation of 1,3-dioxep-5-ene

Abstract

ASJC Scopus subject areas

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