Correction to “Highly Regioselective Synthesis of Oxindolyl-Pyrroles and Quinolines via a One-Pot, Sequential Meyer–Schuster Rearrangement, Anti-Michael Addition/C(sp3)–H Functionalization, and Azacyclization”
Main Authors: | Srinivasarao Yaragorla, Ravikrishna Dada, P. Rajesh, Manju Sharma |
---|---|
Format: | Article |
Language: | English |
Published: |
American Chemical Society
2018-04-01
|
Series: | ACS Omega |
Online Access: | http://dx.doi.org/10.1021/acsomega.8b00578 |
Similar Items
-
Highly Regioselective Synthesis of Oxindolyl-Pyrroles and Quinolines via a One-Pot, Sequential Meyer–Schuster Rearrangement, Anti-Michael Addition/C(sp3)–H Functionalization, and Azacyclization
by: Srinivasarao Yaragorla, et al.
Published: (2018-03-01) -
The Mechanism of the Meyer-Schuster Rearrangement
by: Roane, Carol Virginia
Published: (1976) -
Amine-Triggered Highly Facile Oxidative Benzannulation Reaction for the Synthesis of Anthranilates under Solvent-Free Calcium(II) Catalysis
by: Srinivasarao Yaragorla, et al.
Published: (2017-08-01) - Methodology for the Olefination of Aldehydes and Ketones via the Meyer-Schuster Reaction
-
A one-pot multicomponent reaction for the synthesis of oligoetherols with azacyclic rings
by: Jacek Marek Lubczak, et al.
Published: (2017-12-01)