Self-Mediated Stereoselective Oxidation of Thia-Capped Cyclodextrins

2009 ◽  
Vol 121 (25) ◽  
pp. 4625-4628 ◽  
Author(s):  
Dominique Armspach ◽  
Dominique Matt ◽  
Loic Toupet
Keyword(s):  
Stereoselective Oxidation ◽  
Capped Cyclodextrins

Self-Mediated Stereoselective Oxidation of Thia-Capped Cyclodextrins

2009 ◽  
Vol 48 (25) ◽  
pp. 4555-4558 ◽  
Author(s):  
Dominique Armspach ◽  
Dominique Matt ◽  
Loic Toupet
Keyword(s):  
Stereoselective Oxidation ◽  
Capped Cyclodextrins

Chemo-, Regio-, and Stereoselective Oxidation of the Monocyclic Diterpenoid β-Cembrenediol by P450 BM3

ACS Catalysis ◽  
2015 ◽  
Vol 5 (3) ◽  
pp. 1772-1780 ◽  
Author(s):  
Priska Le-Huu ◽  
Tanja Heidt ◽  
Birgit Claasen ◽  
Sabine Laschat ◽  
Vlada B. Urlacher
Keyword(s):  
P450 Bm3 ◽  
Stereoselective Oxidation

Stereoselective Oxidation of Aryl-Substituted Vicinal Diols into Chiral α-Hydroxy Aldehydes by Re-Engineered Propanediol Oxidoreductase

ACS Catalysis ◽  
2013 ◽  
Vol 3 (12) ◽  
pp. 3016-3025 ◽  
Author(s):  
Cecilia Blikstad ◽  
Käthe M. Dahlström ◽  
Tiina A. Salminen ◽  
Mikael Widersten
Keyword(s):  
Vicinal Diols ◽  
Hydroxy Aldehydes ◽  
Stereoselective Oxidation

The stereoselective oxidation of para‐substituted benzenes by a cytochrome P450 biocatalyst.

2021 ◽  
Author(s):  
Rebecca R. Chao ◽  
Ian C.-K. Lau ◽  
Tom Coleman ◽  
Luke R. Churchman ◽  
Stella A Child ◽  
...  
Keyword(s):  
Cytochrome P450 ◽  
Substituted Benzenes ◽  
Stereoselective Oxidation

The Stereoselective Oxidation of 1-Benzylnicotinium Bromide to Its 1'-N-Oxide

Heterocycles ◽  
1984 ◽  
Vol 22 (2) ◽  
pp. 307 ◽  
Author(s):  
Makoto Shibagaki ◽  
Hajime Matsushita ◽  
Hajime Kaneko
Keyword(s):  
Stereoselective Oxidation

scholarly journals Bioprocess Intensification Using Flow Reactors: Stereoselective Oxidation of Achiral 1,3-diols with Immobilized Acetobacter Aceti

Catalysts ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 208 ◽  
Author(s):  
Valerio De Vitis ◽  
Federica Dall’Oglio ◽  
Francesca Tentori ◽  
Martina Contente ◽  
Diego Romano ◽  
...  
Keyword(s):  
Flow Reactor ◽  
Immobilized Cells ◽  
Reaction Times ◽  
Acetobacter Aceti ◽  
Batch Mode ◽  
Flow Reactors ◽  
Liquid Transfer ◽  
Gas Liquid Flow ◽  
High Yields ◽  
Stereoselective Oxidation

Enantiomerically enriched 2-hydroxymethylalkanoic acids were prepared by oxidative desymmetrisation of achiral 1,3-diols using immobilized cells of Acetobacter aceti in water at 28 °C. The biotransformations were first performed in batch mode with cells immobilized in dry alginate, furnishing the desired products with high molar conversion and reaction times ranging from 2 to 6 h. The biocatalytic process was intensified using a multiphasic flow reactor, where a segmented gas–liquid flow regime was applied for achieving an efficient O2-liquid transfer; the continuous flow systems allowed for high yields and high biocatalyst productivity.

Stereoselective oxidation of cyclopropenes to acyclic enones

1971 ◽  
Vol 12 (49) ◽  
pp. 4761-4764 ◽  
Author(s):  
Louis E. Friedrich ◽  
Russell A. Cormier
Keyword(s):  
Stereoselective Oxidation

Synthesis and stereoselective oxidation of α-thio-β-chloropropenyloxazolidin-2-ones

2010 ◽  
Vol 21 (20) ◽  
pp. 2550-2558 ◽  
Author(s):  
Marie Kissane ◽  
Maureen Murphy ◽  
Simon E. Lawrence ◽  
Anita R. Maguire
Keyword(s):  
Stereoselective Oxidation
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