Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2008
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Resumo |
The Suzuki-Miyaura cross-coupling reaction of a hydroxylated vinyl bromide obtained by a chemoenzymatic approach with a diverse range of potassium organotrifluoroborates has been accomplished catalyzed by Pd(PPh(3))(4) in satisfactory yields. A variety of functional groups are tolerated in the nucleophilic partner. (C) 2008 Elsevier B.V. All rights reserved. |
Identificador |
JOURNAL OF ORGANOMETALLIC CHEMISTRY, v.693, n.6, p.1136-1142, 2008 0022-328X http://producao.usp.br/handle/BDPI/19728 10.1016/j.jorganchem.2008.01.006 |
Idioma(s) |
eng |
Publicador |
ELSEVIER SCIENCE SA |
Relação |
Journal of Organometallic Chemistry |
Direitos |
restrictedAccess Copyright ELSEVIER SCIENCE SA |
Palavras-Chave | #Suzuki-Miyaura cross-coupling reaction #potassium organotrifluoroborate salts #conduritol nucleus #biocatalysis #CROSS-COUPLING REACTIONS #CHEMOENZYMATIC SYNTHESIS #EFFICIENT SYNTHESIS #VINYLIC TELLURIDES #ALKENYL BROMIDES #NATURAL-PRODUCTS #CHEMISTRY #ARYL #SALTS #ACIDS #Chemistry, Inorganic & Nuclear #Chemistry, Organic |
Tipo |
article original article publishedVersion |