Oxalyl chloride as a practical carbon monoxide source for carbonylation reactions

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Standard

Oxalyl chloride as a practical carbon monoxide source for carbonylation reactions. / Hansen, Steffen V F; Ulven, Trond.

In: Organic Letters, Vol. 17, No. 11, 05.06.2015, p. 2832-2835.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Hansen, SVF & Ulven, T 2015, 'Oxalyl chloride as a practical carbon monoxide source for carbonylation reactions', Organic Letters, vol. 17, no. 11, pp. 2832-2835. https://doi.org/10.1021/acs.orglett.5b01252

APA

Hansen, S. V. F., & Ulven, T. (2015). Oxalyl chloride as a practical carbon monoxide source for carbonylation reactions. Organic Letters, 17(11), 2832-2835. https://doi.org/10.1021/acs.orglett.5b01252

Vancouver

Hansen SVF, Ulven T. Oxalyl chloride as a practical carbon monoxide source for carbonylation reactions. Organic Letters. 2015 Jun 5;17(11):2832-2835. https://doi.org/10.1021/acs.orglett.5b01252

Author

Hansen, Steffen V F ; Ulven, Trond. / Oxalyl chloride as a practical carbon monoxide source for carbonylation reactions. In: Organic Letters. 2015 ; Vol. 17, No. 11. pp. 2832-2835.

Bibtex

@article{59ba141b5bfb47ed9fabab80df35fb49,
title = "Oxalyl chloride as a practical carbon monoxide source for carbonylation reactions",
abstract = "A method for generation of high-quality carbon monoxide by decomposition of oxalyl chloride in an aqueous hydroxide solution is described. The usefulness of the method is demonstrated in the synthesis of heterocycles and for hydroxy-, alkoxy-, amino-, and reductive carbonylation reactions, in several cases under milder conditions than previously reported.",
author = "Hansen, {Steffen V F} and Trond Ulven",
year = "2015",
month = jun,
day = "5",
doi = "10.1021/acs.orglett.5b01252",
language = "English",
volume = "17",
pages = "2832--2835",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "11",

}

RIS

TY - JOUR

T1 - Oxalyl chloride as a practical carbon monoxide source for carbonylation reactions

AU - Hansen, Steffen V F

AU - Ulven, Trond

PY - 2015/6/5

Y1 - 2015/6/5

N2 - A method for generation of high-quality carbon monoxide by decomposition of oxalyl chloride in an aqueous hydroxide solution is described. The usefulness of the method is demonstrated in the synthesis of heterocycles and for hydroxy-, alkoxy-, amino-, and reductive carbonylation reactions, in several cases under milder conditions than previously reported.

AB - A method for generation of high-quality carbon monoxide by decomposition of oxalyl chloride in an aqueous hydroxide solution is described. The usefulness of the method is demonstrated in the synthesis of heterocycles and for hydroxy-, alkoxy-, amino-, and reductive carbonylation reactions, in several cases under milder conditions than previously reported.

U2 - 10.1021/acs.orglett.5b01252

DO - 10.1021/acs.orglett.5b01252

M3 - Journal article

VL - 17

SP - 2832

EP - 2835

JO - Organic Letters

JF - Organic Letters

SN - 1523-7060

IS - 11

ER -

ID: 189161616