Organic Letters

, том 13 , издание 10 , страницы 2746-2749

Zinc Triflate Catalyzed Aerobic Cross-Dehydrogenative Coupling (CDC) of Alkynes with Nitrones: A New Entry to Isoxazoles

Тип публикации: Journal Article

Дата публикации: 2011-04-19

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Organic Letters

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SJR: 1.007

CiteScore: 7.7

Impact factor: 4.7

ISSN: 15237060, 15237052

DOI: 10.1021/ol200849k

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PubMed ID: 21504206

Organic Chemistry

Biochemistry

Physical and Theoretical Chemistry

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A mild, operationally simple cross-dehydrogenative coupling between nitrones and terminal alkynes is described by using cheap, readily available 3,3',5,5'-tetra-tert-butyldipheno-quinone and dioxygen as oxidants. These cross-couplings can be performed on various nitrones and alkynes with good to excellent yields. Product nitrones are readily transformed to pharmaceutically important 3,5-disubstituted isoxazoles.

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Murarka S., Studer A. Zinc Triflate Catalyzed Aerobic Cross-Dehydrogenative Coupling (CDC) of Alkynes with Nitrones: A New Entry to Isoxazoles // Organic Letters. 2011. Vol. 13. No. 10. pp. 2746-2749.

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TY - JOUR

DO - 10.1021/ol200849k

UR - https://doi.org/10.1021/ol200849k

TI - Zinc Triflate Catalyzed Aerobic Cross-Dehydrogenative Coupling (CDC) of Alkynes with Nitrones: A New Entry to Isoxazoles

T2 - Organic Letters

AU - Murarka, Sandip

AU - Studer, Armido

PY - 2011

DA - 2011/04/19

PB - American Chemical Society (ACS)

SP - 2746-2749

IS - 10

VL - 13

PMID - 21504206

SN - 1523-7060

SN - 1523-7052

ER -

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@article{2011_Murarka,

author = {Sandip Murarka and Armido Studer},

title = {Zinc Triflate Catalyzed Aerobic Cross-Dehydrogenative Coupling (CDC) of Alkynes with Nitrones: A New Entry to Isoxazoles},

journal = {Organic Letters},

year = {2011},

volume = {13},

publisher = {American Chemical Society (ACS)},

month = {apr},

url = {https://doi.org/10.1021/ol200849k},

number = {10},

pages = {2746--2749},

doi = {10.1021/ol200849k}

}

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Murarka, Sandip, and Armido Studer. “Zinc Triflate Catalyzed Aerobic Cross-Dehydrogenative Coupling (CDC) of Alkynes with Nitrones: A New Entry to Isoxazoles.” Organic Letters, vol. 13, no. 10, Apr. 2011, pp. 2746-2749. https://doi.org/10.1021/ol200849k.

Издатель

American Chemical Society (ACS)

Журнал

Organic Letters

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Tоп 10% SCImago

WOS Q1

БС1