Synthesis

Catalytic Meerwein-Ponndorf-Verley (MPV) and Oppenauer (OPP) reactions: Remarkable acceleration of the hydride transfer by powerful bidentate aluminum …

T Ooi, T Miura, Y Itagaki, H Ichikawa, K Maruoka

Index: Synthesis, , # 2 p. 279 - 291

Full Text: HTML

Citation Number: 47

Abstract

... Synthesis 2002(2): 0279-0291 DOI: 10.1055/s-2002-19802. FEATUREARTICLE. © Georg Thieme Verlag Stuttgart · New York Catalytic Meerwein-Ponndorf-Verley (MPV) and Oppenauer (OPP) Reactions: Remarkable Acceleration ...

Related Articles:

Clean and selective oxidation of aromatic alcohols using silica-supported Jones' reagent in a pressure-driven flow reactor

[Tetrahedron Letters, , vol. 47, # 30 p. 5261 - 5264]

Photo-arbuzov rearrangements of dimethyl benzyl and dimethyl p-acetylbenzyl phosphite

[Journal of the American Chemical Society, , vol. 121, # 10 p. 2085 - 2096]

Efficient and highly selective oxidation of primary alcohols to aldehydes by N-chlorosuccinimide mediated by oxoammonium salts

[Journal of Organic Chemistry, , vol. 61, # 21 p. 7452 - 7454]

Simultaneous functional group manipulation in the Meerwein-Ponndorf-Verley reduction process catalyzed by bidentate aluminum reagent

[Tetrahedron Letters, , vol. 40, # 11 p. 2137 - 2138]

Reversing the Reactivity of Carbonyl Functions with Phosphonium Salts: Enantioselective Total Synthesis of (+)??Centrolobine

[Angewandte Chemie - International Edition, , vol. 50, # 51 p. 12232 - 12235]

More Articles...