نتایج جستجو برای: stereoselective

تعداد نتایج: 4707  

Journal: :Organic letters 2016
Yuji Ochi Satoshi Yokoshima Tohru Fukuyama

The total synthesis of lycopalhine A has been accomplished. The synthesis features construction of the tricyclic system via cleavage of a cyclopropane ring and an ensuing intramolecular Michael addition, stereoselective introduction of a 2-aminoethyl moiety via a reaction of allyltrimethylsilane to a sulfonyliminium ion, and a stereoselective intramolecular aldol reaction.

Journal: :Chemical communications 2013
Jomy Joseph Florian Jaroschik K V Radhakrishnan Jean-Luc Vasse Jan Szymoniak

Allyltitanocene complexes can be generated by reacting pentafulvenes with DIBAL-H and Cp2TiCl2. Their coupling with aldehydes affords homoallylic alcohols in a highly regio- and stereoselective manner. The potential of this method for the stereoselective synthesis of cyclopentane derivatives is illustrated.

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2006
Kent L Kunze Wendel L Nelson Evan D Kharasch Kenneth E Thummel Nina Isoherranen

Itraconazole (ITZ) has three chiral centers and is administered clinically as a mixture of four stereoisomers. This study evaluated stereoselectivity in ITZ metabolism. In vitro experiments were carried out using heterologously expressed CYP3A4. Only (2R,4S,2'R)-ITZ and (2R,4S,2'S)-ITZ were metabolized by CYP3A4 to hydroxy-ITZ, keto-ITZ, and N-desalkyl-ITZ. When (2S,4R,2'R)-ITZ or (2S,4R,2'S)-I...

2016
Jennifer E. Sager Lauren S. L. Price Nina Isoherranen

Bupropion is a widely used antidepressant, smoking cessation aid, and weight-loss therapy. It is administered as a racemic mixture, but the pharmacokinetics and activity of bupropion are stereoselective. The activity and side effects of bupropion are attributed to bupropion and its metabolites S,S- and R,R-OH-bupropion, threohydrobupropion, and erythrohydrobupropion. Yet the stereoselective met...

Journal: :Chemical Science 2023

Rhenium-catalyzed stereoselective transposition of allylic alcohols is reported.

Journal: :Chemical Communications 2021

Regio and stereoselective addition of a phosphine-borane to alkynyl vinyl gold(i) complexes.

Journal: :iranian journal of pharmaceutical research 0
gabriel hancu university of medicine and pharmacy targu mures, faculty of pharmacy, department of pharmaceutical chemistry anca cârje university of medicine and pharmacy targu mures, faculty of pharmacy, department of analytical chemistry ileana iuga university of medicine and pharmacy, faculty of pharmacy, department of pharmaceutical chemistry ibolya fülöp university of medicine and pharmacy targu mures, faculty of pharmacy, department of toxicology and biofarmacy zoltán istvan szabó university of medicine and pharmacy targu mures, faculty of pharmacy, department of pharmaceutical chemistry

carvedilol is administered as a racemic mixture of the r(+)- and s(-)-enantiomers, although it was demonstrated that the two enantiomers exhibit different pharmacological effects and stereoselective pharmacokinetics. the aim of this study was the evaluation of several native and derivatized cyclodextrines as chiral selectors for the separation of carvedilol enantiomers. stereoselective interact...

Journal: :Chemical communications 2015
Thomas O Ronson Martin H H Voelkel Richard J K Taylor Ian J S Fairlamb

The stereoselective synthesis of a challenging macrocyclic polyene scaffold, containing a sensitive vinyl ether motif, has been accomplished using O,C-dilithiation/selective C-alkylation, Pd-catalysed etherification and Wittig reactions as key steps. An end-game macrocyclisation strategy employed a regio- and stereoselective Stille cross-coupling using Pd(Br)(N-Succ)(AsPh3)2 (AsCat) as the prec...

Journal: :Organic & biomolecular chemistry 2008
Natalia Nieto Ian J Munslow Jonathan Barr J Benet-Buchholz Anton Vidal-Ferran

A study, via isotopic labeling, of the stereoselective processes in a Shi-type epoxidation, has revealed that the chiral platform provided by the catalyst mediates the transfer of the pro-S "O" of the related dioxirane species to the alkene in a doubly stereoselective manner.

Journal: :Organic & biomolecular chemistry 2012
V Narasimharao Thota Jacquelyn Gervay-Hague Suvarn S Kulkarni

Synthesis of β-C-D-galactosyl D- and L-alanines is carried out via a highly stereoselective Grignard reaction of glycosyl iodides, Sharpless dihydroxylation and S(N)2 displacement of the corresponding mesylate or tosylate. Alternatively, attempted triflation of the intermediate alcohols triggers a stereoselective debenzylative cyclization leading to interesting bicyclic trans-fused compounds.

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