Water-soluble cobalt(III) porphyrin complexes were found to promote the hydration of terminal alkynes to give methyl ketones. The alkyne hydration proceeded in good to excellent yield with 0.1 to 2 mol % cobalt catalyst <b>1</b> and was compatible with the presence of acid/base- or redox-sensitive functional groups such as alkyl silyl ethers; allyl ethers; trityl ethers; benzyl ethers; carboxylic esters; boronic esters; carboxamides; nitriles; and nitro, iodo, and acetal groups. Some of the alkyne substrates tested here are otherwise difficult to hydrate. The alkyne hydration can be performed on a gram scale, and the catalyst can be recovered by aqueous workup
The NHC-Au-OTf [NHC = 1,3-bis(2,6-di-isopropylphenyl)-imidazol-2-ylidene] catalyst was tested in t...
L−Au−X [L = 1,3-bis(2,6-di-isopropylphenyl)-imidazol-2-ylidene {NHCiPr}, tris(3,5-bis(trifluoromethy...
Alkylarylalkynes are converted with full regioselectivity into the corresponding arylketones by form...
Water-soluble cobalt(III) porphyrin complexes were found to promote the hydration of terminal alkyn...
Cobaloxime (Co(dmgBF(2))(2)center dot 2H(2)O), an inexpensive first-row transition-metal complex, ca...
The review describes the state of the art in hydration reactions of alkynes by direct or indirect ca...
The hydration of aromatic terminal alkynes performed in acetic acid in the presence of catalytic hyd...
A neutral gold(I) complex [(IPr)AuCl] (IPr = 1,3-bis(diisopropylphenyl)imidazol-2-ylidene) was f...
SnCl4·5H2O is a highly efficient catalyst in the hydration of terminal alkynes that affords carbonyl...
Our work shows that simple alkynes can be hydrated by the AuCl/MeOH catalyst system to afford the co...
Visible light promoted hydration of a wide scope of alkynes to ketones catalyzed by rhodium(III) por...
A method to generate carbonylic compounds from alkynes under mild and neutral conditions, with excel...
Herein developed mercuric triflate-TMU catalyzed hydration of terminal alkyne is a mild procedure to...
A Markovnikov-type alkyne hydration protocol is presented using 20% CF<sub>3</sub>SO<sub>3</sub>H (T...
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim The hydration of alkynes is one of the most atom-e...
The NHC-Au-OTf [NHC = 1,3-bis(2,6-di-isopropylphenyl)-imidazol-2-ylidene] catalyst was tested in t...
L−Au−X [L = 1,3-bis(2,6-di-isopropylphenyl)-imidazol-2-ylidene {NHCiPr}, tris(3,5-bis(trifluoromethy...
Alkylarylalkynes are converted with full regioselectivity into the corresponding arylketones by form...
Water-soluble cobalt(III) porphyrin complexes were found to promote the hydration of terminal alkyn...
Cobaloxime (Co(dmgBF(2))(2)center dot 2H(2)O), an inexpensive first-row transition-metal complex, ca...
The review describes the state of the art in hydration reactions of alkynes by direct or indirect ca...
The hydration of aromatic terminal alkynes performed in acetic acid in the presence of catalytic hyd...
A neutral gold(I) complex [(IPr)AuCl] (IPr = 1,3-bis(diisopropylphenyl)imidazol-2-ylidene) was f...
SnCl4·5H2O is a highly efficient catalyst in the hydration of terminal alkynes that affords carbonyl...
Our work shows that simple alkynes can be hydrated by the AuCl/MeOH catalyst system to afford the co...
Visible light promoted hydration of a wide scope of alkynes to ketones catalyzed by rhodium(III) por...
A method to generate carbonylic compounds from alkynes under mild and neutral conditions, with excel...
Herein developed mercuric triflate-TMU catalyzed hydration of terminal alkyne is a mild procedure to...
A Markovnikov-type alkyne hydration protocol is presented using 20% CF<sub>3</sub>SO<sub>3</sub>H (T...
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim The hydration of alkynes is one of the most atom-e...
The NHC-Au-OTf [NHC = 1,3-bis(2,6-di-isopropylphenyl)-imidazol-2-ylidene] catalyst was tested in t...
L−Au−X [L = 1,3-bis(2,6-di-isopropylphenyl)-imidazol-2-ylidene {NHCiPr}, tris(3,5-bis(trifluoromethy...
Alkylarylalkynes are converted with full regioselectivity into the corresponding arylketones by form...