Isatins as privileged molecules in design and synthesis of spiro-fused cyclic frameworks

GS Singh, ZY Desta - Chemical Reviews, 2012 - ACS Publications
1. INTRODUCTION Indoline-2, 3-dione or indole-1H-2, 3-dione (Figure 1), commonly known
as isatin, is a well-known natural product found in plants of genus Isatis and in Couropita …

Molecular diversity of spirooxindoles. Synthesis and biological activity

TL Pavlovska, RG Redkin, VV Lipson, DV Atamanuk - Molecular diversity, 2016 - Springer
Spirooxindoles are important synthetic targets possessing extended biological activity and
drug discovery applications. This review focuses on the various strategies for the …

A decade update on solvent and catalyst-free neat organic reactions: a step forward towards sustainability

A Sarkar, S Santra, SK Kundu, A Hajra, GV Zyryanov… - Green …, 2016 - pubs.rsc.org
Particular success has been achieved in the synthesis of new products and in processes
since the twelve principles of “green chemistry” were formulated in the 1990s. These …

Facile one-pot synthesis of novel dispirooxindole-pyrrolidine derivatives and their antimicrobial and anticancer activity against A549 human lung adenocarcinoma …

Y Arun, G Bhaskar, C Balachandran… - Bioorganic & medicinal …, 2013 - Elsevier
Novel dispirooxindole-pyrrolidine derivatives have been synthesized through 1, 3-dipolar
cycloaddition of an azomethine ylide generated from isatin and sarcosine with the …

Diastereo-and enantioselective construction of 3, 3′-pyrrolidinyldispirooxindole framework via catalytic asymmetric 1, 3-dipolar cycloadditions

W Dai, XL Jiang, Q Wu, F Shi, SJ Tu - The Journal of organic …, 2015 - ACS Publications
The first catalytic enantioselective construction of a 3, 3′-pyrrolidinyldispirooxindole
scaffold has been established via organocatalytic asymmetric 1, 3-dipolar cycloadditions of …

New role for photoexcited organic dye, Na2 eosin Y via the direct hydrogen atom transfer (HAT) process in photochemical visible-light-induced synthesis of …

F Mohamadpour - Dyes and Pigments, 2021 - Elsevier
A green multi-component tandem strategy for metal-free synthesizing spiroacenaphthylenes
and 1H-pyrazolo [1, 2-b] phthalazine-5, 10-diones by Knoevenagel-Michael …

[HTML][HTML] Spirooxindoles: recent report of green synthesis approach

AR Liandi, AH Cahyana, DN Alfariza, R Nuraini… - Green Synthesis and …, 2024 - Elsevier
Spirooxindole is a compound with a unique framework and broad bioactivities in medicine.
In this study, we have reviewed various approaches or methods in synthesizing …

Conjugate Umpolung of β, β‐Disubstituted Enals by Dual Catalysis with an N‐Heterocyclic Carbene and a Brønsted Acid: Facile Construction of Contiguous …

JL Li, B Sahoo, CG Daniliuc… - Angewandte Chemie …, 2014 - Wiley Online Library
A sterically hindered homoenolate has been generated by the NHC‐catalyzed conjugate
umpolung of β, β‐disubstituted enals and successfully employed in a facile stereoselective …

Diastereo‐and Enantioselective Construction of a Bispirooxindole Scaffold Containing a Tetrahydro‐β‐carboline Moiety through an Organocatalytic Asymmetric …

W Dai, H Lu, X Li, F Shi, SJ Tu - Chemistry–A European …, 2014 - Wiley Online Library
The first catalytic asymmetric construction of a new class of bispirooxindole scaffold‐
containing tetrahydro‐β‐carboline moiety has been established through chiral phosphoric …

Catalytic asymmetric synthesis of 3, 3-disubstituted oxindoles: diazooxindole joins the field

ZY Cao, YH Wang, XP Zeng, J Zhou - Tetrahedron Letters, 2014 - Elsevier
The catalytic asymmetric synthesis of 3, 3-disubstituted oxindoles, a big family of privileged
scaffolds in natural products and drugs, is of current interest. Recently, the catalytic …