A synergistic‐catalysis‐enabled reaction of 2‐indolymethanols with oxonium ylides has
been established that makes use of a three‐component reaction between 3‐diazooxindoles …

A Ag/P-stereogenic phosphine-complex-catalyzed 1, 3-dipolar cycloaddition of azomethine
ylides with electron-deficient olefins is reported. In this reaction, highly functionalized …

Arynes are highly reactive intermediates, which are utilized for the electrophilic arylation of
various X–H bonds (X= O, N, S etc.). Herein, a new synthetic strategy is demonstrated …

Highly regio-and diastereoselective syntheses of a new set of functionalized pyrrolidines,
spiro-pyrrolidine/pyrrolizidine oxindoles, spiroacenaphthylenolyl-pyrrolidines/pyrrolizidines …

This paper reveals the diastereoselective Pd‐catalyzed intramolecular α‐C (sp3)− H
arylation in amides. The intermolecular and intramolecular α‐arylation of tertiary C (sp3)− H …

The acetic acid promoted reaction of 3-hydroxy-3-(indol-3-yl) indolin-2-ones and mercapto-
substituted β-enamino esters showed very interesting molecular diversity. The reaction in …

The In (OTf) 3-catalyzed α-vinylation of various hydroxy-functionalized quaternary carbon
centers using in situ generated isobutylene from tert-butyl acetate is presented as a novel …

The first Sc (OTf) 3-catalyzed dehydration of 2-hydroxy oxime ethers to generate benzylic
stabilized 1-azaallyl cations, which are captured by 1, 3-carbonyls, is described. A …

Lewis‐acid‐catalysed reaction of 3‐hydroxy‐2‐oxindoles with a variety of terminal alkynes
has been developed. The key step involves alkylation of 3‐aryl (or) 3‐alkyl, 3 …

Alkynyl-3-OBoc oxindoles underwent Cu (II) mediated Friedel-Crafts alkylation with indoles
and phenols to yield of structurally diverse 3-alkynyl-3-indole/phenol-oxindole derivatives …