A synthesis of alkynyl azacycloalkanes by the coupling reaction of alkynyl boranes and lactams

Masahiko Yamaguchi; Ichiro Hirao

doi:10.1016/S0040-4039(00)81753-0

A synthesis of alkynyl azacycloalkanes by the coupling reaction of alkynyl boranes and lactams

Masahiko Yamaguchi, Ichiro Hirao

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

33 Citations (Scopus)

Abstract

Alkynyl azacycloalkanes are synthesized in good yields by the addition reactionn of alkynyl boranes to lactams followed by a lithium aluminum hydride reduction of the adducts.

Original language	English
Pages (from-to)	1719-1722
Number of pages	4
Journal	Tetrahedron Letters
Volume	24
Issue number	16
DOIs	https://doi.org/10.1016/S0040-4039(00)81753-0
Publication status	Published - 1983
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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title = "A synthesis of alkynyl azacycloalkanes by the coupling reaction of alkynyl boranes and lactams",

abstract = "Alkynyl azacycloalkanes are synthesized in good yields by the addition reactionn of alkynyl boranes to lactams followed by a lithium aluminum hydride reduction of the adducts.",

author = "Masahiko Yamaguchi and Ichiro Hirao",

year = "1983",

doi = "10.1016/S0040-4039(00)81753-0",

language = "English",

volume = "24",

pages = "1719--1722",

journal = "Tetrahedron Letters",

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AU - Yamaguchi, Masahiko

AU - Hirao, Ichiro

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Y1 - 1983

N2 - Alkynyl azacycloalkanes are synthesized in good yields by the addition reactionn of alkynyl boranes to lactams followed by a lithium aluminum hydride reduction of the adducts.

AB - Alkynyl azacycloalkanes are synthesized in good yields by the addition reactionn of alkynyl boranes to lactams followed by a lithium aluminum hydride reduction of the adducts.

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U2 - 10.1016/S0040-4039(00)81753-0

DO - 10.1016/S0040-4039(00)81753-0

M3 - Article

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 16

ER -

A synthesis of alkynyl azacycloalkanes by the coupling reaction of alkynyl boranes and lactams

Abstract

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