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 …

Recent contributions from the Baylis− Hillman reaction to organic chemistry

D Basavaiah, BS Reddy, SS Badsara - Chemical reviews, 2010 - ACS Publications
Organic synthesis is one of the most successful and useful disciplines of science and mainly
involves the construction of carbon-carbon bond (s) and carbon-heteroatom bond (s) and …

Advances in the Baylis–Hillman reaction-assisted synthesis of cyclic frameworks

V Singh, S Batra - Tetrahedron, 2008 - Elsevier
Acquiring the capability to access structurally complex and diverse molecules through
simple starting substrates has been one of the underlying principles of chemical research …

Diastereodivergent synthesis of 3‐spirocyclopropyl‐2‐oxindoles through direct enantioselective cyclopropanation of oxindoles

X Dou, Y Lu - Chemistry–A European Journal, 2012 - Wiley Online Library
Oxindoles are structural motifs that are widely present in natural products and medicinally
important agents.[1] In particular, spirocyclic oxindoles bearing a quaternary stereogenic …

Catalytic asymmetric synthesis of polysubstituted spirocyclopropyl oxindoles: organocatalysis versus transition metal catalysis

ZY Cao, J Zhou - Organic Chemistry Frontiers, 2015 - pubs.rsc.org
Spirocyclopropyl oxindoles are widely present in natural products and bioactive molecules.
In addition, they play a significant role as a type of donor–acceptor (DA) cyclopropanes in …

Synthesis of novel functionalized 3-spiropyrrolizidine and 3-spiropyrrolidine oxindoles from baylis− hillman adducts of isatin and heteroaldehydes with azomethine …

P Shanmugam, B Viswambharan, S Madhavan - Organic Letters, 2007 - ACS Publications
Synthesis of Novel Functionalized 3-Spiropyrrolizidine and 3-Spiropyrrolidine Oxindoles
from Baylis−Hillman Adducts of Isatin and Heteroaldehydes with Azomethine Ylides via [3+2]-Cycloaddition …

Recent progress on routes to spirooxindole systems derived from isatin

M Xia, RZ Ma - Journal of Heterocyclic Chemistry, 2014 - Wiley Online Library
Because of their definite or potential biological and pharmaceutical activities, spirooxindole
heterocycles have been widely studied, and there has occurred a research boom on routes …

Enantioselective Morita− Baylis− Hillman Reaction of Isatins with Acrylates: Facile Creation of 3-Hydroxy-2-oxindoles

F Zhong, GY Chen, Y Lu - Organic Letters, 2011 - ACS Publications
The first tertiary amine catalyzed enantioselective Morita− Baylis− Hillman (MBH) reaction of
isatins with acrylates has been demonstrated, allowing asymmetric synthesis of biologically …

A new vinyl selenone-based domino approach to spirocyclopropyl oxindoles endowed with anti-HIV RT activity

M Palomba, L Rossi, L Sancineto… - Organic & …, 2016 - pubs.rsc.org
Herein, we disclose a general and flexible access to spirocyclopropyl oxindoles by a domino
Michael/intramolecular nucleophilic substitution pathway with variously substituted vinyl …

Pyridine Core Activation via 1,5-Electrocyclization of Vinyl Pyridinium Ylides Generated from Bromo Isomerized Morita−Baylis−Hillman Adduct of Isatin and Pyridine …

B Viswambharan, K Selvakumar, S Madhavan… - Organic …, 2010 - ACS Publications
An activation of the pyridine nucleus has been achieved via 1, 5-electrocyclization of vinyl
pyridinium ylides generated from bromo isomerized Morita− Baylis− Hillman adducts of …