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ChemInform Abstract: Enantioselective Reduction of Prochiral Ketones Catalyzed by New (R)-4- (Phenylmercapto)methyl-5,5-diphenyl-1,3,2-oxazaborolidine and Bis-((R, R)-5,5-diphenyl-1,3,2-oxazaborolidine methyl)disulfide from L-Cystine.

✍ Scribed by X. LI; R. XIE


Publisher
John Wiley and Sons
Year
2010
Weight
31 KB
Volume
28
Category
Article
ISSN
0931-7597

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Remote Control of Diels-Alder Additions. Enantioselective Synthesis of (2R)-1,2,3,4-Tetrahydro-2-hydroxy-5,8-dimethoxynaphthalen-2-yl Methyl Ketone (Wong's Anthracycline Intermediate) from Furfural. -The Diels-Alder reaction of (II) with vinyl ester (III) proceeds with high regioselectivity but low