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Volume 10, Number 24, 17 December 1999

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Steric effects in the enantioselective transfer hydrogenation of 2-aroylacetates
pp. 4663-4666(4)
Authors: Everaere K.; Carpentier J.-F.; Mortreux A.; Bulliard M.

Asymmetric acyloin condensation catalyzed by phenylpyruvate decarboxylase
pp. 4667-4675(9)
Authors: Guo Z.; Goswami A.; Mirfakhrae K.D.; Patel R.N.

Highly stereocontrolled boron-mediated synthesis of beta-hydroxy-alpha-amino acids and dipeptides. Part 2
pp. 4709-4714(6)
Authors: Di Felice P.; Maestri M.; Paradisi F.; Porzi G.; Sandri S.

Microbiological reductions of chromen-4-one derivatives
pp. 4745-4754(10)
Authors: Besse P.; Baziard-Mouysset G.; Boubekeur K.; Palvadeau P.; Veschambre H.; Payard M.; Mousset G.

Enzymatic resolution of a 1,2-cyclic sulphite glycerol derivative
pp. 4755-4762(8)
Authors: Lemaire M.; Bolte J.

Facile synthesis of enantiopure 1,1'-binaphthyl-2,2'-dicarboxylic acid via lipase-catalyzed kinetic resolution
pp. 4763-4768(6)
Authors: Furutani T.; Hatsuda M.; Imashiro R.; Seki M.

Asymmetric benzoin reaction catalyzed by benzoylformate decarboxylase
pp. 4769-4774(6)
Authors: Demir A.S.; Dunnwald T.; Iding H.; Pohl M.; Muller M.

Chemo-enzymatic preparation from renewable resources of enantiopure 1,3-oxazolidine-2-thiones
pp. 4775-4780(6)
Authors: Leoni O.; Bernardi R.; Gueyrard D.; Rollin P.; Palmieri S.

Asymmetric hydrogenation of indene carboxylic acids: stereochemistry of hydrogen addition
pp. 4781-4789(9)
Authors: Borszeky K.; Mallat T.; Baiker A.

Transformation of (+)-thiomicamine into a new ligand for the enantioselective addition of methyllithium to prochiral imines
pp. 4791-4796(6)
Authors: Brozda D.; Chrzanowska M.; Gluszynska A.; Rozwadowska M.D.

[1,2]-Wittig rearrangement of acetals. Part 1: Investigation about structural requirements
pp. 4811-4830(20)
Authors: Gartner P.; Letschnig M.F.; Knollmuller M.; Vollenkle H.

Stereoselective synthesis of 2-azetidinones as cholesterol-absorption inhibitors
pp. 4841-4849(9)
Authors: Annunziata R.; Benaglia M.; Cinquini M.; Cozzi F.

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