Synthesis of substituted biarylmethanol via ferrocenyloxime palladacycles catalyzed suzuki reaction of chlorophenylmethanol in water
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Li, Hong-Mei,Feng, Ai-Qing,Lou, Xin-Hua
p. 2551 - 2554
(2014/09/17)
Synthesis of biaryls by intramolecular radical transfer in phosphinates
Phosphinates 20a-35a give biaryls 20b-35b on heating with stannanes in the presence of AIBN. The process involves a radical ipso substitution on the migrating aryl ring.
Clive,Kang
p. 6083 - 6091
(2007/10/03)
Synthesis of biaryls by intramolecular radical transfer: Use of phosphinates
Phosphinates 4a-13a give biaryls 4b-13b on heating with stannanes in the presence of a radical initiator. (C) 2000 Elsevier Science Ltd.
Clive, Derrick L.J.,Kang, Shunzhen
p. 1315 - 1319
(2007/10/03)
A Palladium Mediated Spiroketal Synthesis
The synthesis of a variety of spiroketal-containing systems is outlined, utilising a palladium catalysed coupling reaction in the pivotal carbon-carbon bond forming step.
Elsley, David A.,MacLeod, Donald,Miller, John A.,Quayle, Peter,Davies, Gareth M.
p. 409 - 412
(2007/10/02)
Conformational Study of Anticholinesterase Carbamates in the Furylbenzene Series by 1H and 13C NMR Spectroscopy
The structural analysis of carbamates derived from 2-(α-furyl)benzaldoximes and 2-(α-furyl)benzyl alcohols was carried out by 1H and 13C NMR spectroscopy.The conjugative and steric effects of alkyl substituents introduced on the benzene rings were found to modify the relative orientation of the aromatic and furan rings.The existence of a close relationship between the stereochemistry of the studied compounds and their anticholinesterase activity has been proposed.
Platzer, N.,Ronzani, N.,Lang, C.,Lange, C.
p. 14 - 19
(2007/10/02)
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