A convenient two step protocol for the synthesis of cyclopentenones and indanones, including an asymmetric variant

Daniel J. Kerr; Christiane Metje; Bernard L. Flynn

doi:10.1039/b211845a

A convenient two step protocol for the synthesis of cyclopentenones and indanones, including an asymmetric variant

Daniel J. Kerr, Christiane Metje, Bernard L. Flynn^*

^*Corresponding author for this work

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

70 Citations (Scopus)

Abstract

A one-pot palladium mediated hydrostannylation/cross-coupling protocol is used to give direct access to cross-conjugated dienones that can be utilized in Nazarov cyclizations to afford highly substituted cyclopentenones and indanones, including an asymmetric variant.

Original language	English
Pages (from-to)	1380-1381
Number of pages	2
Journal	Chemical Communications
Volume	3
Issue number	12
DOIs	https://doi.org/10.1039/b211845a
Publication status	Published - 2003

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title = "A convenient two step protocol for the synthesis of cyclopentenones and indanones, including an asymmetric variant",

abstract = "A one-pot palladium mediated hydrostannylation/cross-coupling protocol is used to give direct access to cross-conjugated dienones that can be utilized in Nazarov cyclizations to afford highly substituted cyclopentenones and indanones, including an asymmetric variant.",

author = "{J. Kerr}, Daniel and Christiane Metje and {L. Flynn}, Bernard",

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AB - A one-pot palladium mediated hydrostannylation/cross-coupling protocol is used to give direct access to cross-conjugated dienones that can be utilized in Nazarov cyclizations to afford highly substituted cyclopentenones and indanones, including an asymmetric variant.

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U2 - 10.1039/b211845a

DO - 10.1039/b211845a

M3 - Article

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SP - 1380

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JO - Chemical Communications

JF - Chemical Communications

IS - 12

ER -

A convenient two step protocol for the synthesis of cyclopentenones and indanones, including an asymmetric variant

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