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Tuesday, April 28, 2020 | History

2 edition of HLADH-catalysed reduction of trans-(1,3,3a,6,7,7a) hexahydro-5-(4 H)-benzo [C]-thiopheneone. found in the catalog.

HLADH-catalysed reduction of trans-(1,3,3a,6,7,7a) hexahydro-5-(4 H)-benzo [C]-thiopheneone.

Iain Alexander Gair

HLADH-catalysed reduction of trans-(1,3,3a,6,7,7a) hexahydro-5-(4 H)-benzo [C]-thiopheneone.

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Published .
Written in English


The Physical Object
Pagination74 leaves
Number of Pages74
ID Numbers
Open LibraryOL16344684M


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HLADH-catalysed reduction of trans-(1,3,3a,6,7,7a) hexahydro-5-(4 H)-benzo [C]-thiopheneone. by Iain Alexander Gair Download PDF EPUB FB2

Horse liver alcohol dehydrogenase (HLADH) catalysed reduction of a series of ortho- and meta-substituted benzaldehyde chromium tricarbonyl complexes has been studied.

Enzymatic Reduction Reaction. In book: Asymmetric Organic Synthesis with Enzymes, pp (HLADH) catalysed reduction of a series of ortho- and meta-substituted benzaldehyde chromium. Optically active tetrahydropyranol was obtained by the horse liver alcohol dehydrogenase (HLADH)-catalysed reduction of tetrahydropyranone, and the corresponding brosylate was prepared.

Acetolysis of the optically active brosylate gave racemic 3-tetrahydropyranyl acetate as well as varying amounts of Cited by: 1. Optically active tetrahydropyranol was obtained by the horse liver alcohol dehydrogenase (HLADH)-catalysed reduction of tetrahydropyranone, and the corresponding brosylate was prepared.

Acetolysis of the optically active brosylate gave racemic 3-tetrahydropyranyl acetate as well as varying amounts of racemic.