Catalytic non‐enzymatic kinetic resolution
H Pellissier - Advanced Synthesis & Catalysis, 2011 - Wiley Online Library
While tremendous advances have been made in asymmetric synthesis, the resolution of
racemates is still the most important industrial approach to the synthesis of chiral …
racemates is still the most important industrial approach to the synthesis of chiral …
Enantioselective cobalt-catalyzed transformations
H Pellissier, H Clavier - Chemical reviews, 2014 - ACS Publications
1. INTRODUCTION The catalysis of organic reactions by metals still constitutes one of the
most useful and powerful tools in organic synthesis. 1 Although asymmetric synthesis is …
most useful and powerful tools in organic synthesis. 1 Although asymmetric synthesis is …
Ni/photoredox-catalyzed enantioselective cross-electrophile coupling of styrene oxides with aryl iodides
A Ni/photoredox-catalyzed enantioselective reductive coupling of styrene oxides and aryl
iodides is reported. This reaction affords access to enantioenriched 2, 2-diarylalcohols from …
iodides is reported. This reaction affords access to enantioenriched 2, 2-diarylalcohols from …
A Nuclearity‐Dependent Enantiodivergent Epoxide Opening via Enthalpy‐Controlled Mononuclear and Entropy‐Controlled Dinuclear (Salen) Titanium Catalysis
S Li, H Zhu, L Li, W Chen, J Jiang, ZW Qu… - Angewandte …, 2023 - Wiley Online Library
A nuclearity‐dependent enantiodivergent epoxide opening reaction has been developed, in
which both antipodes of chiral alcohol products are selectively accessed by mononuclear …
which both antipodes of chiral alcohol products are selectively accessed by mononuclear …
A green chemistry approach to asymmetric catalysis: solvent-free and highly concentrated reactions
PJ Walsh, H Li, CA de Parrodi - Chemical reviews, 2007 - ACS Publications
In an age when organic chemists have shown that even the most complex natural and
unnatural products can be synthesized, 1-3 the emphasis of synthetic chemistry is shifting to …
unnatural products can be synthesized, 1-3 the emphasis of synthetic chemistry is shifting to …
Fluorinated cycloalkyl building blocks for drug discovery
OO Grygorenko, KP Melnykov, S Holovach… - …, 2022 - Wiley Online Library
The review covers various aspects of fluorinated cycloalkyl (C3− C7) building blocks for drug
discovery, including their synthesis, key physicochemical properties, and biological and …
discovery, including their synthesis, key physicochemical properties, and biological and …
Enantioselective Cross-Coupling of meso-Epoxides with Aryl Halides
Y Zhao, DJ Weix - Journal of the American Chemical Society, 2015 - ACS Publications
The first enantioselective cross-electrophile coupling of aryl bromides with meso-epoxides to
form trans-β-arylcycloalkanols is presented. The reaction is catalyzed by a combination of …
form trans-β-arylcycloalkanols is presented. The reaction is catalyzed by a combination of …
MIL‐101‐SO3H: A Highly Efficient Brønsted Acid Catalyst for Heterogeneous Alcoholysis of Epoxides under Ambient Conditions
YX Zhou, YZ Chen, Y Hu, G Huang… - … A European Journal, 2014 - Wiley Online Library
For the first time, a∼ 100% sulfonic acid functionalized metal–organic framework (MOF), MIL‐
101‐SO3H, with giant pores has been prepared by a hydrothermal process followed by a …
101‐SO3H, with giant pores has been prepared by a hydrothermal process followed by a …
Click chemistry-what's in a name? Triazole synthesis and beyond
The environmentally amiable route to carbon-heteroatom bond formation, described by
Sharpless as 'click chemistry', has become known as a fast, efficient, and reliable approach …
Sharpless as 'click chemistry', has become known as a fast, efficient, and reliable approach …
Stereoselective anhydride openings
I Atodiresei, I Schiffers, C Bolm - Chemical reviews, 2007 - ACS Publications
Desymmetrization of meso compounds to yield chiral products proved to be a powerful
synthetic tool in asymmetric synthesis since it allows formation of multiple stereogenic …
synthetic tool in asymmetric synthesis since it allows formation of multiple stereogenic …