Development of general catalytic allylation of acylhydrazones with pinacolyl allylboronate using an indium(I) catalyst

Uwe Schneider; I-Hon Chen; Shu Kobayashi

doi:10.1021/ol702756k

Development of general catalytic allylation of acylhydrazones with pinacolyl allylboronate using an indium(I) catalyst

Uwe Schneider, I-Hon Chen, Shu Kobayashi

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Abstract / Description of output

Catalytic allylation of various acylhydrazones using a group 13 metal reagent (boron) in combination with a group 13 metal catalyst in its low-oxidation state (indium) has been developed. This operationally simple carbon-carbon bond-forming reaction displays remarkable substrate scope and functional group tolerance.

Original language	English
Pages (from-to)	737-740
Number of pages	4
Journal	Organic letters
Volume	10
Issue number	5
DOIs	https://doi.org/10.1021/ol702756k
Publication status	Published - 6 Mar 2008

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http://pubs.acs.org/doi/abs/10.1021/ol702756k

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@article{0f1e377f4ad84d75a524232af164ea6b,

title = "Development of general catalytic allylation of acylhydrazones with pinacolyl allylboronate using an indium(I) catalyst",

abstract = "Catalytic allylation of various acylhydrazones using a group 13 metal reagent (boron) in combination with a group 13 metal catalyst in its low-oxidation state (indium) has been developed. This operationally simple carbon-carbon bond-forming reaction displays remarkable substrate scope and functional group tolerance.",

author = "Uwe Schneider and I-Hon Chen and Shu Kobayashi",

year = "2008",

month = mar,

day = "6",

doi = "10.1021/ol702756k",

language = "English",

volume = "10",

pages = "737--740",

journal = "Organic letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "5",

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T1 - Development of general catalytic allylation of acylhydrazones with pinacolyl allylboronate using an indium(I) catalyst

AU - Schneider, Uwe

AU - Chen, I-Hon

AU - Kobayashi, Shu

PY - 2008/3/6

Y1 - 2008/3/6

N2 - Catalytic allylation of various acylhydrazones using a group 13 metal reagent (boron) in combination with a group 13 metal catalyst in its low-oxidation state (indium) has been developed. This operationally simple carbon-carbon bond-forming reaction displays remarkable substrate scope and functional group tolerance.

AB - Catalytic allylation of various acylhydrazones using a group 13 metal reagent (boron) in combination with a group 13 metal catalyst in its low-oxidation state (indium) has been developed. This operationally simple carbon-carbon bond-forming reaction displays remarkable substrate scope and functional group tolerance.

U2 - 10.1021/ol702756k

DO - 10.1021/ol702756k

M3 - Article

SN - 1523-7060

VL - 10

SP - 737

EP - 740

JO - Organic letters

JF - Organic letters

IS - 5

ER -

Development of general catalytic allylation of acylhydrazones with pinacolyl allylboronate using an indium(I) catalyst

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