Acid-catalyzed synthesis of methylene-bridged (S)-tyrosine−phenol dimers

Sean P. Bew; David L. Hughes; Sunil Sharma

doi:10.1021/jo0610863

Acid-catalyzed synthesis of methylene-bridged (S)-tyrosine−phenol dimers

Sean P. Bew, David L. Hughes, Sunil Sharma

Chemistry of Materials and Catalysis

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

10 Citations (Scopus)

Abstract

The efficient synthesis of 2,2‘-arylmethylene dimers from 3-hydroxymethyl or 3-methoxymethyl-5-halo-(S)-tyrosines and para-substituted phenols under acid-catalyzed reaction conditions using either conventional or microwave-assisted protocols is described.

Original language	English
Pages (from-to)	7881-7884
Number of pages	4
Journal	Journal of Organic Chemistry
Volume	71
Issue number	20
DOIs	https://doi.org/10.1021/jo0610863
Publication status	Published - 29 Sep 2006

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title = "Acid-catalyzed synthesis of methylene-bridged (S)-tyrosine−phenol dimers",

abstract = "The efficient synthesis of 2,2{\textquoteleft}-arylmethylene dimers from 3-hydroxymethyl or 3-methoxymethyl-5-halo-(S)-tyrosines and para-substituted phenols under acid-catalyzed reaction conditions using either conventional or microwave-assisted protocols is described.",

author = "Bew, {Sean P.} and Hughes, {David L.} and Sunil Sharma",

year = "2006",

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day = "29",

doi = "10.1021/jo0610863",

language = "English",

volume = "71",

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journal = "Journal of Organic Chemistry",

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T1 - Acid-catalyzed synthesis of methylene-bridged (S)-tyrosine−phenol dimers

AU - Bew, Sean P.

AU - Hughes, David L.

AU - Sharma, Sunil

PY - 2006/9/29

Y1 - 2006/9/29

N2 - The efficient synthesis of 2,2‘-arylmethylene dimers from 3-hydroxymethyl or 3-methoxymethyl-5-halo-(S)-tyrosines and para-substituted phenols under acid-catalyzed reaction conditions using either conventional or microwave-assisted protocols is described.

AB - The efficient synthesis of 2,2‘-arylmethylene dimers from 3-hydroxymethyl or 3-methoxymethyl-5-halo-(S)-tyrosines and para-substituted phenols under acid-catalyzed reaction conditions using either conventional or microwave-assisted protocols is described.

UR - http://www.scopus.com/inward/record.url?scp=33749135701&partnerID=8YFLogxK

U2 - 10.1021/jo0610863

DO - 10.1021/jo0610863

M3 - Article

VL - 71

SP - 7881

EP - 7884

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 20

ER -

Acid-catalyzed synthesis of methylene-bridged (S)-tyrosine−phenol dimers

Abstract

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