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

72 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.",

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doi = "10.1039/b211845a",

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T1 - A convenient two step protocol for the synthesis of cyclopentenones and indanones, including an asymmetric variant

AU - J. Kerr, Daniel

AU - Metje, Christiane

AU - L. Flynn, Bernard

PY - 2003

Y1 - 2003

N2 - 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.

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.

UR - https://www.scopus.com/pages/publications/0038378999

U2 - 10.1039/b211845a

DO - 10.1039/b211845a

M3 - Article

SN - 1359-7345

VL - 3

SP - 1380

EP - 1381

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

Abstract

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