Ru(ii)-Catalyzed spirocyclization of aryl N-sulfonyl ketimines with aryl isocyanates through an aromatic C–H bond activation-Reference-Cited by-同舟云学术

Ru(ii)-Catalyzed spirocyclization of aryl N-sulfonyl ketimines with aryl isocyanates through an aromatic C–H bond activation

Published:2018 Issue:14 Volume:16 Page:2522-2526
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

K. Nagarjuna Reddy¹²³⁴⁵^ORCID,U. Subhadra¹²³⁴,B. Sridhar⁶²³⁴,B. V. Subba Reddy¹²³⁴^ORCID

Affiliation:

1. Centre for Semiochemicals

2. CSIR-Indian Institute of Chemical Technology

3. Hyderabad – 500 007

4. India

5. Academy of Scientific and Innovative Research (AcSIR)

6. Laboratory of X-ray Crystallography

Abstract

A novel one-pot strategy has been developed for the construction of spiro-isoindolinone-benzosultams through a Ru(ii)-catalyzed sequential C–C and C–N bond formation.

Funder

Council for Scientific and Industrial Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C7OB03198J

Reference62 articles.

1. Sc(OTf)3-catalyzed three-component cascade reaction: One-pot synthesis of substituted 3-oxoisoindoline-1-carbonitrile derivatives

2. Palladium-Catalysed Heteroannulation with Terminal Alkynes: a Highly Regio- and Stereoselective Synthesis of (Z)-3-Aryl(alkyl)idene Isoindolin-1-ones

3. Transition metal free intramolecular selective oxidative C(sp3)–N coupling: synthesis of N-aryl-isoindolinones from 2-alkylbenzamides

4. Facile ligand-free Pd-catalyzed tandem C–C/C–N coupling reaction: a novel access to highly diverse tetrazole tag isoindoline derivatives

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