ChemInform Abstract: Regio- and Enantioselective Reduction of Diketones: Preparation of Enantiomerically Pure Hydroxy Ketones Catalyzed by Candida parapsilosis ATCC 7330.

ChemInform ◽  
2016 ◽  
Vol 47 (14) ◽  
Author(s):  
Pula Mahajabeen ◽  
Anju Chadha
Keyword(s):  
Candida Parapsilosis ◽  
Enantiomerically Pure ◽  
Enantioselective Reduction ◽  
Hydroxy Ketones ◽  
Candida Parapsilosis Atcc 7330

Enantio- & chemo-selective preparation of enantiomerically enriched aliphatic nitro alcohols using Candida parapsilosis ATCC 7330

RSC Advances ◽  
2015 ◽  
Vol 5 (90) ◽  
pp. 73807-73813 ◽  
Author(s):  
Sowmyalakshmi Venkataraman ◽  
Anju Chadha
Keyword(s):  
Candida Parapsilosis ◽  
Asymmetric Reduction ◽  
Reaction Conditions ◽  
Enantiomerically Pure ◽  
Candida Parapsilosis Atcc 7330

Enantiomerically pure β- and γ-nitro alcohols were prepared from their respective nitro ketones by asymmetric reduction using Candida parapsilosis ATCC 7330 under optimized reaction conditions (ee up to >99%; yields up to 76%).

Regio- and enantio-selective oxidation of diols by Candida parapsilosis ATCC 7330

RSC Advances ◽  
2014 ◽  
Vol 4 (105) ◽  
pp. 60526-60533 ◽  
Author(s):  
Thakkellapati Sivakumari ◽  
Anju Chadha
Keyword(s):  
Selective Oxidation ◽  
Candida Parapsilosis ◽  
Whole Cells ◽  
Hydroxy Ketones ◽  
Candida Parapsilosis Atcc 7330 ◽  
Optically Pure

Optically pure (S)-diols and their corresponding hydroxy ketones were prepared via regio- and enantio-selective oxidation of the corresponding diols using whole cells of Candida parapsilosis ATCC 7330.

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