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Transition metal catalyzed aerobic asymmetric coupling of 2-naphthols. / Tkachenko, Nikolay V.; Bryliakov, Konstantin P.

In: Mini-Reviews in Organic Chemistry, Vol. 16, No. 4, 01.01.2019, p. 392-398.

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Tkachenko NV, Bryliakov KP. Transition metal catalyzed aerobic asymmetric coupling of 2-naphthols. Mini-Reviews in Organic Chemistry. 2019 Jan 1;16(4):392-398. doi: 10.2174/1570193X15666180418153713

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Tkachenko, Nikolay V. ; Bryliakov, Konstantin P. / Transition metal catalyzed aerobic asymmetric coupling of 2-naphthols. In: Mini-Reviews in Organic Chemistry. 2019 ; Vol. 16, No. 4. pp. 392-398.

BibTeX

@article{3fc1d57d8d1b4f9ebbc21bd983264b6b,
title = "Transition metal catalyzed aerobic asymmetric coupling of 2-naphthols",
abstract = "Optically pure 1,1′-bi-2-naphthol (BINOL) and its derivatives are among the most widely used chiral ligands and auxiliaries for asymmetric synthesis. These molecules also occur as scaffolds for various biologically active compounds. Direct oxidative coupling of 2-naphthols in the presence of chiral catalysts provides a powerful strategy for the synthesis of optically pure 1,1′-bi-2-naphthols (BINOLS). In 1978, Wynberg with co-workers discovered that a copper salt with chiral auxiliary mediates the oxidative coupling of 2-naphthols, which can be taken as the starting point for further progress in this area. Over the last decades, a number of efficient and stereoselective catalyst systems have been developed. This mini-review surveys the aerobic asymmetric oxidative coupling of 2-naphthols catalyzed by transition metal complexes reported since 1995.",
keywords = "2-naphthol, Aerobic oxidative coupling, Asymmetric synthesis, BINOL, Mechanism, Transition metals",
author = "Tkachenko, {Nikolay V.} and Bryliakov, {Konstantin P.}",
note = "Publisher Copyright: {\textcopyright} 2019 Bentham Science Publishers.",
year = "2019",
month = jan,
day = "1",
doi = "10.2174/1570193X15666180418153713",
language = "English",
volume = "16",
pages = "392--398",
journal = "Mini-Reviews in Organic Chemistry",
issn = "1570-193X",
publisher = "Bentham Science Publishers B.V.",
number = "4",

}

RIS

TY - JOUR

T1 - Transition metal catalyzed aerobic asymmetric coupling of 2-naphthols

AU - Tkachenko, Nikolay V.

AU - Bryliakov, Konstantin P.

N1 - Publisher Copyright: © 2019 Bentham Science Publishers.

PY - 2019/1/1

Y1 - 2019/1/1

N2 - Optically pure 1,1′-bi-2-naphthol (BINOL) and its derivatives are among the most widely used chiral ligands and auxiliaries for asymmetric synthesis. These molecules also occur as scaffolds for various biologically active compounds. Direct oxidative coupling of 2-naphthols in the presence of chiral catalysts provides a powerful strategy for the synthesis of optically pure 1,1′-bi-2-naphthols (BINOLS). In 1978, Wynberg with co-workers discovered that a copper salt with chiral auxiliary mediates the oxidative coupling of 2-naphthols, which can be taken as the starting point for further progress in this area. Over the last decades, a number of efficient and stereoselective catalyst systems have been developed. This mini-review surveys the aerobic asymmetric oxidative coupling of 2-naphthols catalyzed by transition metal complexes reported since 1995.

AB - Optically pure 1,1′-bi-2-naphthol (BINOL) and its derivatives are among the most widely used chiral ligands and auxiliaries for asymmetric synthesis. These molecules also occur as scaffolds for various biologically active compounds. Direct oxidative coupling of 2-naphthols in the presence of chiral catalysts provides a powerful strategy for the synthesis of optically pure 1,1′-bi-2-naphthols (BINOLS). In 1978, Wynberg with co-workers discovered that a copper salt with chiral auxiliary mediates the oxidative coupling of 2-naphthols, which can be taken as the starting point for further progress in this area. Over the last decades, a number of efficient and stereoselective catalyst systems have been developed. This mini-review surveys the aerobic asymmetric oxidative coupling of 2-naphthols catalyzed by transition metal complexes reported since 1995.

KW - 2-naphthol

KW - Aerobic oxidative coupling

KW - Asymmetric synthesis

KW - BINOL

KW - Mechanism

KW - Transition metals

UR - http://www.scopus.com/inward/record.url?scp=85063740892&partnerID=8YFLogxK

U2 - 10.2174/1570193X15666180418153713

DO - 10.2174/1570193X15666180418153713

M3 - Review article

AN - SCOPUS:85063740892

VL - 16

SP - 392

EP - 398

JO - Mini-Reviews in Organic Chemistry

JF - Mini-Reviews in Organic Chemistry

SN - 1570-193X

IS - 4

ER -

ID: 19355518