Palladium-catalyzed coupling reaction of vinyl epoxides, diol acetonides, and diol carbonates with organobismuth compounds

S. K. Kang; H. C. Ryu; Y. T. Hong; M. S. Kim; S. W. Lee; J. H. Jung

doi:10.1081/SCC-100104838

Palladium-catalyzed coupling reaction of vinyl epoxides, diol acetonides, and diol carbonates with organobismuth compounds

S. K. Kang
, H. C. Ryu
, Y. T. Hong
, M. S. Kim
, S. W. Lee
, J. H. Jung

Department of Biological Sciences

Sungkyunkwan University

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

28 Scopus citations

Abstract

The palladium-catalyzed arylation reaction of vinyl epoxides with organobismuth compounds afforded the aryl-substituted (E)-allylic alcohols via ring opening of epoxides. Alternatively, the palladium-catalyzed reaction of diol acetonides and carbonates with bismuth derivatives afforded the aryl-substituted diol acetonides and carbonates without ring opening.

Original language	English
Pages (from-to)	2365-2371
Number of pages	7
Journal	Synthetic Communications
Volume	31
Issue number	15
DOIs	https://doi.org/10.1081/SCC-100104838
State	Published - 2001

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title = "Palladium-catalyzed coupling reaction of vinyl epoxides, diol acetonides, and diol carbonates with organobismuth compounds",

abstract = "The palladium-catalyzed arylation reaction of vinyl epoxides with organobismuth compounds afforded the aryl-substituted (E)-allylic alcohols via ring opening of epoxides. Alternatively, the palladium-catalyzed reaction of diol acetonides and carbonates with bismuth derivatives afforded the aryl-substituted diol acetonides and carbonates without ring opening.",

author = "Kang, \{S. K.\} and Ryu, \{H. C.\} and Hong, \{Y. T.\} and Kim, \{M. S.\} and Lee, \{S. W.\} and Jung, \{J. H.\}",

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doi = "10.1081/SCC-100104838",

language = "English",

volume = "31",

pages = "2365--2371",

journal = "Synthetic Communications",

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T1 - Palladium-catalyzed coupling reaction of vinyl epoxides, diol acetonides, and diol carbonates with organobismuth compounds

AU - Kang, S. K.

AU - Ryu, H. C.

AU - Hong, Y. T.

AU - Kim, M. S.

AU - Lee, S. W.

AU - Jung, J. H.

PY - 2001

Y1 - 2001

N2 - The palladium-catalyzed arylation reaction of vinyl epoxides with organobismuth compounds afforded the aryl-substituted (E)-allylic alcohols via ring opening of epoxides. Alternatively, the palladium-catalyzed reaction of diol acetonides and carbonates with bismuth derivatives afforded the aryl-substituted diol acetonides and carbonates without ring opening.

AB - The palladium-catalyzed arylation reaction of vinyl epoxides with organobismuth compounds afforded the aryl-substituted (E)-allylic alcohols via ring opening of epoxides. Alternatively, the palladium-catalyzed reaction of diol acetonides and carbonates with bismuth derivatives afforded the aryl-substituted diol acetonides and carbonates without ring opening.

UR - https://www.scopus.com/pages/publications/0034897094

U2 - 10.1081/SCC-100104838

DO - 10.1081/SCC-100104838

M3 - Article

AN - SCOPUS:0034897094

SN - 0039-7911

VL - 31

SP - 2365

EP - 2371

JO - Synthetic Communications

JF - Synthetic Communications

IS - 15

ER -

Palladium-catalyzed coupling reaction of vinyl epoxides, diol acetonides, and diol carbonates with organobismuth compounds

Abstract

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