Results 111 to 120 of about 27,319 (289)

Improving the Stereoselectivity of Bakers' Yeast Reductions by Genetic Engineering

open access: yes, 2016
The stereoselectivities of bakers' yeast catalyzed reductions of β-keto esters can be manipulated by genetic design. Strains in which two major β-keto ester reductases are either knocked out or overexpressed have been constructed.
Jon D. Stewart (1323831)   +2 more
core   +1 more source

Regio- and stereoselective synthesis of new diaminocyclopentanols

open access: yesBeilstein Journal of Organic Chemistry, 2014
The optimal conditions for regio- and stereoselective epoxide ring opening of N,N-disubstituted 1,2-epoxy-3-aminocyclopentanes by different nucleophilic reagents have been developed.
Evgeni A. Larin   +2 more
doaj   +1 more source

Unpicking the Cause of Stereoselectivity in Actinorhodin Ketoreductase Variants with Atomistic Simulations

open access: yes, 2018
Ketoreductase enzymes (KRs) with a high degree of regio- and stereoselectivity are useful biocatalysts for the production of small, specific chiral alcohols from achiral ketones.
Marc, van der Kamp   +1 more
core   +1 more source

Sulfur‐Directed Construction of Vinyl Cyclopropanes from 1,3‐Dienes

open access: yesAngewandte Chemie International Edition, EarlyView.
Sulfur takes control. A pending thioether acts as a molecular compass, directing carbene addition to the 1,3‐diene scaffold with exceptional regio‑ and diastereocontrol to forge sulfur‐substituted vinyl cyclopropanes (S‐VCPs) — molecular architectures inaccessible via conventional cyclopropanation strategies.
Anna Keimer   +6 more
wiley   +1 more source

Stereoselectivity of the interaction of muscarinic antagonists with their receptors

open access: yes, 1989
The stereoselectivity of the interaction with muscarinic receptors of enantiomers of a series of chiral antagonists is receptor subtype dependent. There is no overall relationship between stereoselectivity and receptor affinity.
Christophe, Jean   +8 more
core  

Tertiary alcohol preferred: Hydroxylation of trans-3-methyl-L-proline with proline hydroxylases

open access: yesBeilstein Journal of Organic Chemistry, 2011
The enzymatic synthesis of tertiary alcohols by the stereospecific oxidation of tertiary alkyl centers is a most-straightforward but challenging approach, since these positions are sterically hindered.
Christian Klein, Wolfgang Hüttel
doaj   +1 more source

Stereoselectivity in Glycosylation with Deoxofluorinated Glucosazide and Galactosazide Thiodonors

open access: yes, 2019
Control of anomeric stereoselectivity in glycosylation with deoxofluorinated glycosyl donors is critical for assembly of fluorinated oligosaccharides. Here, we report the synthesis of benzylated 3-fluoro and 4-fluoro analogues of phenyl 1-thioglucosazide
Monika Müllerová (6671789)   +13 more
core   +1 more source

Molecular Basis for the Substrate Stereoselectivity in Tryptophan Dioxygenase

open access: yes, 2016
Tryptophan dioxygenase (TDO) and indoleamine 2,3-dioxygenase (IDO) are the only two heme proteins that catalyze the oxidation reaction of tryptophan (Trp) to N-formylkynurenine.
Dario A. Estrin (120783)   +4 more
core   +1 more source

Radical synthesis of biaryls and dihydrobiaryls: Controlling stereoselectivity in rhamnopyranosylation.

open access: yes, 2007
Radical synthesis of biaryls and dihydrobiaryls: Controlling stereoselectivity in ...
Miteshkumar. Patel (7977485)
core  

Origin of the Relative Stereoselectivity of the β-Lactam Formation in the Staudinger Reaction

open access: yes, 2016
The relative (cis, trans) stereoselectivity of the β-lactam formation is one of the critical issues in the Staudinger reaction. Although many attempts have been made to explain and to predict the stereochemical outcomes, the origin of the ...
Lei Jiao (780172)   +2 more
core   +1 more source

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