Results 131 to 140 of about 23,776 (268)

Practical Enantioselective Approach to 3‐Amino‐2‐Hydroxy Acids and Application to the Synthesis of Natural Products

Chirality, Volume 38, Issue 7, July 2026.
A practical and straightforward approach to optically active erythro 3‐amino‐2‐hydroxy acids and its application to the enantioselective synthesis of 3‐phenylisoserine and of the marine natural product 3‐amino‐2‐hydroxy‐6‐methylheptanoic acid is reported.
Marilena Caporale, Giulia Marsico, Ernesto Santoro, Patrizia Scafato, Stefano Superchi   +4 more
wiley   +1 more source

Diastereoselective α- and β-Functionalisation of Cyclic Sulfoximines

, 2022
In this thesis, the diastereoselective α- and β-functionalisation of cyclic sulfoximines via lithiation-trapping and various cross-coupling reactions is described.
Hartley, Giordaina
core  

Photoinduced Hydrogenative Dearomatization With Homocoupling of Quinolines to Construct Octahydro‐4,4'‐biquinolines

Chemistry – A European Journal, Volume 32, Issue 24, 23 June 2026.
Dearomative homocoupling of quinolines into 1,1',2,2',3,3',4,4'‐octahydro‐4,4'‐biquinoline (OHBQ) is reported. The photoexcited boron complex, in situ generated from quinoline, HB(pin), and KOtBu, enables the unprecedented homocoupling of tetrahydroquinolines that is challenging in the ground state, expanding the chemical diversity of OHBQ derivatives.
Mone Suzuki, Asuha Shimose, Yuki Nagashima   +2 more
wiley   +1 more source

Aldehyde–Olefin Couplings by Photoinduced Reduction of Electron‐Deficient Olefins with Hantzsch Ester Anions

Angewandte Chemie, Volume 138, Issue 25, 15 June 2026.
Single‐electron transfer‐mediated reductive carbonyl–olefin couplings are valuable carbon–carbon bond forming reactions. However, limitations persist for couplings of aliphatic aldehydes with electron‐deficient olefins. Here, we report a simple, photocatalyst‐free protocol that overcomes these limitations by using a Hantzsch ester anion as a ...
Zhihang Li, Adam Noble
wiley   +2 more sources

A Highly Enantio- and Diastereoselective Catalytic Intramolecular Stetter Reaction

, 2016
A highly enantio- and diastereoselective intramolecular Stetter reaction has been developed. Subjection of α,α-disubstituted Michael acceptors to an asymmetric intramolecular Stetter reaction results in a highly enantioselective conjugate addition and a ...
Javier Read de Alaniz (675328), Tomislav Rovis (1308306)   +1 more
core   +1 more source

Aziridination of a Single Carbon Atom in Alkenes via Energy Transfer Catalysis

Angewandte Chemie International Edition, Volume 65, Issue 26, 22 June 2026.
Contrary to traditional alkene aziridination via (formal) nitrene transfer, we herein report a strategy that achieves intermolecular aziridination of a single alkene carbon atom and installs an additional group at the other. Enabled by metal‐free energy transfer (EnT) catalysis, alkenyl boronates and silanes are transformed into reactive intermediates ...
Fritz Paulus, Corinna Heusel, Felix H. Wessels, Bünyamin Sikora, Maik G. Niedziella, Kilian van der Beck, Constantin G. Daniliuc, Frank Glorius   +7 more
wiley   +1 more source

Asymmetric Michael Addition of Cyanide to α,β‐Unsaturated Aldehydes Catalyzed by Diarylmethyl‐Substituted Diphenylprolinol Silyl Ethers: Thermodynamically Controlled Product Formation under Kinetic Enantioselective Catalysis

Advanced Synthesis &Catalysis, Volume 368, Issue 12, 17 June 2026.
Asymmetric Michael addition of cyanide to α,β‐unsaturated aldehydes catalyzed by diarylmethyl‐substituted diphenylprolinol silyl ethers:Thermodynamically controlled product formation under kinetic enantioselective catalysis. Diphenylprolinol silyl ether catalyzed asymmetric Michael/1,2‐addition reaction of cyanide to α,β‐unsaturated aldehydes at high ...
Konstantinos Daskalakis, Naoki Mori, Satrajit Indu, Riku Fukami, Yujiro Hayashi   +4 more
wiley   +1 more source

Ir-catalyzed diastereoselective isomerization of primary allylic alcohols

, 2015
Efficient enantioselective isomerizations of prochiral allylic alcohols have been independently reported by our group and others in recent years. However, diastereoselective isomerization with chiral substrates had been barely documented. Herein, we have
Li, Houhua
core   +1 more source

1,1‐and 1,2‐Diborylalkenes: Preparation and Synthetic Applications

Advanced Synthesis &Catalysis, Volume 368, Issue 12, 17 June 2026.
In this review, we highlight recent advances in the synthesis and reactivity of 1,1‐diborylalkenes and 1,2‐diborylalkenes, along with various transformations leading to C‐C, C‐heteroatom, and multicomponent products. By providing a comprehensive and practical resource, this review aims to assist researchers in exploring the synthetic utility of 1,1 and
Jayaram Vankudoth, Maruti Mali, Fabienne Berrée   +2 more
wiley   +1 more source

Diastereomeric Amides Derived from Malonic Acid: the Role of Chiral Auxiliaries and of the Nature of Co-Acids in the Mixed Kolbe Electrolyses

Journal of the Brazilian Chemical Society, 1999
Experiments towards the diastereoselective coupling of new malonic acid amides synthesized with commercially available chiral amines [(S)-(+)-1-cyclohexylethylamine and (R)-(+)-1-phenylethylamine] as chiral auxiliaries were performed through Kolbe ...
Goulart Marília O.F., Schäfer Hans-Yürgen   +1 more
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