Palladium catalyzed cyclizations of oxime esters with 1,2-disubstituted alkenes: synthesis of dihydropyrroles

Nicholas J Race; J. F. Bower

doi:10.1021/ol4023112

Palladium catalyzed cyclizations of oxime esters with 1,2-disubstituted alkenes: synthesis of dihydropyrroles

Nicholas J Race, J. F. Bower

Research output: Contribution to journal › Article (Academic Journal) › peer-review

66 Citations (Scopus)

Abstract

Pd-catalyzed cyclizations of oxime esters with 1,2-dialkylated alkenes provide an entry to chiral dihydropyrroles. Substrate and catalyst controlled strategies for selective product formation (vs alternative pyrroles) are outlined.

Original language	English
Pages (from-to)	4616-4619
Journal	Organic Letters
Volume	15
DOIs	https://doi.org/10.1021/ol4023112
Publication status	Published - 2013

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3-month Core Capability for Chemistry Research
Crosby, J.
1/01/13 → 1/04/13
Project: Research
New Transition Metal Catalysed Methods for Alkyl C-N Bond Formation
Bower, J. F.
3/11/11 → 3/11/13
Project: Research

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title = "Palladium catalyzed cyclizations of oxime esters with 1,2-disubstituted alkenes: synthesis of dihydropyrroles",

abstract = "Pd-catalyzed cyclizations of oxime esters with 1,2-dialkylated alkenes provide an entry to chiral dihydropyrroles. Substrate and catalyst controlled strategies for selective product formation (vs alternative pyrroles) are outlined.",

author = "Race, {Nicholas J} and Bower, {J. F.}",

year = "2013",

doi = "10.1021/ol4023112",

language = "English",

volume = "15",

pages = "4616--4619",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

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AU - Race, Nicholas J

AU - Bower, J. F.

PY - 2013

Y1 - 2013

N2 - Pd-catalyzed cyclizations of oxime esters with 1,2-dialkylated alkenes provide an entry to chiral dihydropyrroles. Substrate and catalyst controlled strategies for selective product formation (vs alternative pyrroles) are outlined.

AB - Pd-catalyzed cyclizations of oxime esters with 1,2-dialkylated alkenes provide an entry to chiral dihydropyrroles. Substrate and catalyst controlled strategies for selective product formation (vs alternative pyrroles) are outlined.

U2 - 10.1021/ol4023112

DO - 10.1021/ol4023112

M3 - Article (Academic Journal)

C2 - 23981032

SN - 1523-7060

VL - 15

SP - 4616

EP - 4619

JO - Organic Letters

JF - Organic Letters

ER -

Palladium catalyzed cyclizations of oxime esters with 1,2-disubstituted alkenes: synthesis of dihydropyrroles

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3-month Core Capability for Chemistry Research

New Transition Metal Catalysed Methods for Alkyl C-N Bond Formation

Cite this