Oxalyl chloride as a practical carbon monoxide source for carbonylation reactions
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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
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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