Palladium catalysed alkylative dimerization between pronucleophiles and vinyltins

Itaru Nakamura; Naofumi Tsukada; Mohammad Al-Masum; Yoshinori Yamamoto

doi:10.1039/a703463f

Palladium catalysed alkylative dimerization between pronucleophiles and vinyltins

Itaru Nakamura, Naofumi Tsukada, Mohammad Al-Masum, Yoshinori Yamamoto

SCI - Research and Analytical Center for Giant Molecules

Tohoku University

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

3 Citations (Scopus)

Abstract

In the presence of catalytic amounts of Pd₂(dba)₃·CHCl₃ and dppb, the reaction of pronucleophiles 1 with vinyltins 2 gives the corresponding alkylative dimerization products of the vinyl group, 1,4-disubstituted butene derivatives 3, in good to high yields.

Original language	English
Pages (from-to)	1583-1584
Number of pages	2
Journal	Chemical Communications
Issue number	16
DOIs	https://doi.org/10.1039/a703463f
Publication status	Published - 1997

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title = "Palladium catalysed alkylative dimerization between pronucleophiles and vinyltins",

abstract = "In the presence of catalytic amounts of Pd2(dba)3·CHCl3 and dppb, the reaction of pronucleophiles 1 with vinyltins 2 gives the corresponding alkylative dimerization products of the vinyl group, 1,4-disubstituted butene derivatives 3, in good to high yields.",

author = "Itaru Nakamura and Naofumi Tsukada and Mohammad Al-Masum and Yoshinori Yamamoto",

year = "1997",

doi = "10.1039/a703463f",

language = "English",

pages = "1583--1584",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "16",

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T1 - Palladium catalysed alkylative dimerization between pronucleophiles and vinyltins

AU - Nakamura, Itaru

AU - Tsukada, Naofumi

AU - Al-Masum, Mohammad

AU - Yamamoto, Yoshinori

PY - 1997

Y1 - 1997

N2 - In the presence of catalytic amounts of Pd2(dba)3·CHCl3 and dppb, the reaction of pronucleophiles 1 with vinyltins 2 gives the corresponding alkylative dimerization products of the vinyl group, 1,4-disubstituted butene derivatives 3, in good to high yields.

AB - In the presence of catalytic amounts of Pd2(dba)3·CHCl3 and dppb, the reaction of pronucleophiles 1 with vinyltins 2 gives the corresponding alkylative dimerization products of the vinyl group, 1,4-disubstituted butene derivatives 3, in good to high yields.

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UR - http://www.scopus.com/inward/citedby.url?scp=0008130183&partnerID=8YFLogxK

U2 - 10.1039/a703463f

DO - 10.1039/a703463f

M3 - Article

AN - SCOPUS:0008130183

SN - 1359-7345

SP - 1583

EP - 1584

JO - Chemical Communications

JF - Chemical Communications

IS - 16

ER -

Palladium catalysed alkylative dimerization between pronucleophiles and vinyltins

Abstract

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