Baker's yeast mediated reduction of dihydroxyacetone derivatives

J Bálint, G Egri, A Kolbert, C Dianóczky, E Fogassy…

Index: Balint, Jozsef; Egri, Gabriella; Kolbert, Attila; Dianoczky, Csilla; Fogassy, Elemer; Novak, Lajos; Poppe, Laszlo Tetrahedron Asymmetry, 1999 , vol. 10, # 20 p. 4017 - 4028

Full Text: HTML

Citation Number: 20

Abstract

Several monoprotected dihydroxyacetone derivatives 4a–d and their acetates 5a–d were prepared and subjected to biotransformation with baker's yeast. The simple chemical modification of the substrates (ie transforming the relatively small hydrophilic hydroxymethyl group into a larger hydrophobic acetoxymethyl moiety) inverted the sense of enantiotope selectivity of these reductions yielding optically active diols 6a–d, or their enantiomeric ...

Related Articles:

Facile syntheses of L-α-glycerophosphorylcholine

[Park, Jong Moon; De Castro, Kathlia A.; Ahn, Hyunseok; Rhee, Hakjune Bulletin of the Korean Chemical Society, 2010 , vol. 31, # 9 p. 2689 - 2691]

Structure and synthesis of petrosynes, new acetylenic enol ether glycerides from the Okinawan marine sponge of the genus Petrosia

[Iguchi, Kazuo; Kitade, Makoto; Kashiwagi, Toshihiko; Yamada, Yasuji Journal of Organic Chemistry, 1993 , vol. 58, # 21 p. 5690 - 5698]

Synthesis of chiral 2-(4-phenoxyphenylsulfonylmethyl) thiiranes as selective gelatinase inhibitors

[Takano, Seiichi; Seya, Kazuhiko; Goto, Emiko; Hirama, Michiyasu; Ogasawara, Kunio Synthesis, 1983 , # 2 p. 116 - 117]

Efficient chemoenzymatic enantioselective synthesis of diacylglycerols (DAG)

[Guanti, Giuseppe; Banfi, Luca; Basso, Andrea; Bevilacqua, Elisabetta; Bondanza, Laura; Riva, Renata Tetrahedron Asymmetry, 2004 , vol. 15, # 18 p. 2889 - 2892]

Efficient chemoenzymatic enantioselective synthesis of diacylglycerols (DAG)

[Guanti, Giuseppe; Banfi, Luca; Basso, Andrea; Bevilacqua, Elisabetta; Bondanza, Laura; Riva, Renata Tetrahedron Asymmetry, 2004 , vol. 15, # 18 p. 2889 - 2892]

More Articles...