ChemInform Abstract: One-Pot Synthesis of Enantiomerically Pure 1,2-Diols: Asymmetric Reduction of Aromatic α-Oxoaldehydes Catalyzed by Candida parapsilosis ATCC 7330.

ChemInform ◽  
2012 ◽  
Vol 43 (26) ◽  
pp. no-no
Author(s):  
Pula Mahajabeen ◽  
Anju Chadha
Keyword(s):  
Candida Parapsilosis ◽  
Asymmetric Reduction ◽  
One Pot ◽  
Enantiomerically Pure ◽  
One Pot Synthesis ◽  
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%).

Indium Bromide-catalyzed Unprecedented Hydrogenolysis: A Novel One-Pot Synthesis of Per-O-Acetylated β-carboxymethyl O and S-glycosides

2020 ◽  
Vol 24 (8) ◽  
pp. 900-908
Author(s):  
Ram Naresh Yadav ◽  
Amrendra K Singh ◽  
Bimal Banik
Keyword(s):  
Asymmetric Synthesis ◽  
Chiral Auxiliary ◽  
Bioactive Molecules ◽  
One Pot ◽  
Enantiomerically Pure ◽  
Stereoselective Glycosylation ◽  
One Pot Synthesis ◽  
Wide Range

Numerous O (oxa)- and S (thia)-glycosyl esters and their analogous glycosyl acids have been accomplished through stereoselective glycosylation of various peracetylated bromo sugar with benzyl glycolate using InBr3 as a glycosyl promotor followed by in situ hydrogenolysis of resulting glycosyl ester. A tandem glycosylating and hydrogenolytic activity of InBr3 has been successfully investigated in a one-pot procedure. The resulting synthetically valuable and virtually unexplored class of β-CMGL (glycosyl acids) could serve as an excellent potential chiral auxiliary in the asymmetric synthesis of a wide range of enantiomerically pure medicinally prevalent β-lactams and other bioactive molecules of diverse medicinal interest.

ChemInform Abstract: One-Pot Synthesis of Enantiomerically Pure N-Protected Allylic Amines from N-Protected α-Amino Esters.

ChemInform ◽  
2016 ◽  
Vol 47 (36) ◽  
Author(s):  
Gaston Silveira-Dorta ◽  
Sergio J Alvarez-Mendez ◽  
Victor S Martin ◽  
Jose M Padron
Keyword(s):  
Allylic Amines ◽  
One Pot ◽  
Enantiomerically Pure ◽  
Amino Esters ◽  
One Pot Synthesis

One-Pot Synthesis of Novel Enantiomerically Pure and Racemic 4-Ferrocenyl-β-lactams and Their Reactivity in Acidic Media

2005 ◽  
Vol 2005 (15) ◽  
pp. 3326-3333 ◽  
Author(s):  
Luca Bernardi ◽  
Bianca F. Bonini ◽  
Mauro Comes-Franchini ◽  
Gabriella Dessole ◽  
Mariafrancesca Fochi ◽  
...  
Keyword(s):  
Acidic Media ◽  
One Pot ◽  
Enantiomerically Pure ◽  
One Pot Synthesis
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