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

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

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

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

Medicinal Chemistry

Research output: Contribution to journal › Article › Research › 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 he 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	9
Issue number	12
Publication status	Published - 21 Jun 2003

Cite this

@article{46fc94c2052340ca97d3f9d983a4d766,

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 he utilized in Nazarov cyclizations to afford highly substituted cyclopentenones and indanones, including an asymmetric variant.",

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

year = "2003",

month = jun,

day = "21",

language = "English",

volume = "9",

pages = "1380--1381",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "The Royal Society of Chemistry",

number = "12",

}

TY - JOUR

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

AU - Kerr, Daniel J.

AU - Metje, Christiane

AU - Flynn, Bernard L.

PY - 2003/6/21

Y1 - 2003/6/21

N2 - A one-pot palladium mediated hydrostannylation/cross-coupling protocol is used to give direct access to cross-conjugated dienones that can he 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 he utilized in Nazarov cyclizations to afford highly substituted cyclopentenones and indanones, including an asymmetric variant.

UR - http://www.scopus.com/inward/record.url?scp=0038378999&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0038378999

SN - 1359-7345

VL - 9

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

Other files and links

Cite this