Isoindolinone Synthesis via One‐Pot Type Transition Metal Catalyzed C− C Bond Forming Reactions

R Savela, C Méndez‐Gálvez - Chemistry–A European Journal, 2021 - Wiley Online Library
Isoindolinone structure is an important privileged scaffold found in a large variety of naturally
occurring as well as synthetic, biologically and pharmaceutically active compounds. Owing …

Catalytic asymmetric synthesis of isoindolinones

W Gao, M Chen, Q Ding, Y Peng - Chemistry–An Asian Journal, 2019 - Wiley Online Library
As important reactive species, isoindolinones represent a cluster of valuable building blocks
for the construction of natural‐product‐like compounds. In particular, chiral isoindolinones …

Asymmetric synthesis of 3-substituted isoindolinones: Application to the total synthesis of (+)-lennoxamine

DL Comins, S Schilling, Y Zhang - Organic Letters, 2005 - ACS Publications
Asymmetric Synthesis of 3-Substituted Isoindolinones: Application to the Total Synthesis of (+)-Lennoxamine
| Organic Letters ACS ACS Publications C&EN CAS Find my institution Log In Organic …

Hydroxorhodium/chiral diene complexes as effective catalysts for the asymmetric arylation of 3-aryl-3-hydroxyisoindolin-1-ones.

T Nishimura, A Noishiki, Y Ebe… - Angewandte …, 2013 - search.ebscohost.com
The transition-metal-catalyzed enantioselective alkylation and arylation of imines is a
versatile means of accessing α-chiral amines, which are important structural components of …

Asymmetric alkynylation/lactamization cascade: An expeditious entry to enantiomerically enriched isoindolinones

V Bisai, A Suneja, VK Singh - … Chemie International Edition, 2014 - Wiley Online Library
An unprecedented CuI–pybox‐diPh‐catalyzed highly enantioselective (up to> 99% ee)
alkynylation/lactamization cascade has been developed as a general catalytic system for the …

Tunable system for electrochemical reduction of ketones and phthalimides

Y Wang, J Zhao, T Qiao, J Zhang… - Chinese Journal of …, 2021 - Wiley Online Library
Main observation and conclusion Herein, we report an efficient, tunable system for
electrochemical reduction of ketones and phthalimides at room temperature without the …

Asymmetric hydrogenolysis of racemic tertiary alcohols, 3-substituted 3-hydroxyisoindolin-1-ones

MW Chen, QA Chen, Y Duan, ZS Ye… - Chemical …, 2012 - pubs.rsc.org
Asymmetric hydrogenolysis of racemic tertiary alcohols, 3-substituted 3-hydroxyisoindolin-1-
ones, was developed using chiral phosphoric acid as catalyst and a Hantzsch ester as the …

A general catalytic route to isoindolinones and tetrahydroisoquinolines: application in the synthesis of (±)-crispine A

S Dhanasekaran, V Bisai, RA Unhale, A Suneja… - Organic …, 2014 - ACS Publications
An unprecedented highly efficient Lewis acid catalyzed one-pot cascade has been
demonstrated as a general catalytic system for the synthesis of diversely substituted …

A General Catalytic Route to Enantioenriched Isoindolinones and Phthalides: Application in the Synthesis of (S)-PD 172938

SK Ray, MM Sadhu, RG Biswas, RA Unhale… - Organic …, 2019 - ACS Publications
Chiral Brønsted acid catalyzed enantioselective syntheses of isoindolinones and phthalides
have been accomplished via tandem Mannich-lactamization and aldol-lactonization …

An Efficient Entry to syn- and anti-Selective Isoindolinones via an Organocatalytic Direct Mannich/Lactamization Sequence

V Bisai, RA Unhale, A Suneja, S Dhanasekaran… - Organic …, 2015 - ACS Publications
An organocatalytic direct Mannich–lactamization sequence for the syntheses of
pharmacologically important enantioenriched isoindolinones is reported. The method …