Highly regioselective friedländer reaction

Yi Hsiao; Nelo R. Rivera; Nobuyoshi Yasuda; David L. Hughes; Paul J. Reider

doi:10.1021/ol006785v

Highly regioselective friedländer reaction

Yi Hsiao, Nelo R. Rivera, Nobuyoshi Yasuda, David L. Hughes, Paul J. Reider

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

76 Scopus citations

Abstract

Matrix presented A highly regioselective Friedländer reaction is described. By introduction of a phosphonate group at one of the α-carbons of a ketone, regioselectivity can be perfectly controlled.

Original language	English (US)
Pages (from-to)	1101-1103
Number of pages	3
Journal	Organic letters
Volume	3
Issue number	8
DOIs	https://doi.org/10.1021/ol006785v
State	Published - Apr 19 2001
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol006785v

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@article{8b431d612c8e42f38edd56f296568002,

title = "Highly regioselective friedl{\"a}nder reaction",

abstract = "Matrix presented A highly regioselective Friedl{\"a}nder reaction is described. By introduction of a phosphonate group at one of the α-carbons of a ketone, regioselectivity can be perfectly controlled.",

author = "Yi Hsiao and Rivera, {Nelo R.} and Nobuyoshi Yasuda and Hughes, {David L.} and Reider, {Paul J.}",

year = "2001",

month = apr,

day = "19",

doi = "10.1021/ol006785v",

language = "English (US)",

volume = "3",

pages = "1101--1103",

journal = "Organic letters",

issn = "1523-7060",

publisher = "American Chemical Society",

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TY - JOUR

T1 - Highly regioselective friedländer reaction

AU - Hsiao, Yi

AU - Rivera, Nelo R.

AU - Yasuda, Nobuyoshi

AU - Hughes, David L.

AU - Reider, Paul J.

PY - 2001/4/19

Y1 - 2001/4/19

N2 - Matrix presented A highly regioselective Friedländer reaction is described. By introduction of a phosphonate group at one of the α-carbons of a ketone, regioselectivity can be perfectly controlled.

AB - Matrix presented A highly regioselective Friedländer reaction is described. By introduction of a phosphonate group at one of the α-carbons of a ketone, regioselectivity can be perfectly controlled.

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UR - http://www.scopus.com/inward/citedby.url?scp=0035912306&partnerID=8YFLogxK

U2 - 10.1021/ol006785v

DO - 10.1021/ol006785v

M3 - Article

C2 - 11348169

AN - SCOPUS:0035912306

SN - 1523-7060

VL - 3

SP - 1101

EP - 1103

JO - Organic letters

JF - Organic letters

IS - 8

ER -

Highly regioselective friedländer reaction

Abstract

All Science Journal Classification (ASJC) codes

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