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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02299
Abstract: A three-component reaction of alkynes, arylzinc chlorides, and iodomethanes was found to proceed in the presence of a rhodium catalyst to give high yields of trisubstituted/tetrasubstituted alkenes. The usual arylzinc chlorides only gave trisubstituted alkenes,…
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Keywords:
arylzinc chlorides;
reaction alkynes;
component reaction;
migration ... See more keywords
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Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.7b03223
Abstract: Visible-light-induced direct C-H arylation of S,S-functionalized internal alkenes, that is, α-oxo ketene dithioacetals and analogues, has been efficiently realized with aryldiazonium salts (ArN2BF4) as coupling partners and Ru(bpy)3Cl2·6H2O as photosensitizer at ambient temperature. The strategy…
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Keywords:
tetrasubstituted alkenes;
photoredox catalyzed;
arylation;
tamoxifen ... See more keywords
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Published in 2018 at "ACS Omega"
DOI: 10.1021/acsomega.8b02966
Abstract: An operationally simple, efficient, and metal-/peroxide-free three-component reaction of alkynes, iodine, and sodium sulfinates has been developed for the construction of highly functionalized tetrasubstituted alkenes. Iodo- and sulfonyl-containing tetrasubstituted alkenes, such as vinyl ketones, allylic…
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Keywords:
tetrasubstituted alkenes;
iodine sodium;
reaction alkynes;
alkynes iodine ... See more keywords