Rhodium(ii) catalyzed synthesis of macrocycles incorporating oxindole via O–H/N–H insertion reactions-Reference-Cited by-同舟云学术

Rhodium(ii) catalyzed synthesis of macrocycles incorporating oxindole via O–H/N–H insertion reactions

Published:2014 Issue:45 Volume:12 Page:9243-9256
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Muthusamy Sengodagounder¹²³,Karikalan Thangaraju¹²³

Affiliation:

1. School of Chemistry

2. Bharathidasan University

3. Tiruchirappalli 620 024, India

Abstract

Synthesis of 10- to 29-membered oxaza-macrocyclesviaintramolecular O–H/N–H insertion reactions catalyzed by a rhodium(ii) acetate dimer is demonstrated. Synthesis of symmetric macrocyclesviahead to tail dimerization reactions is also delineated.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB01671H

Reference63 articles.

1. M. P. Doyle , M. A.McKervey and T.Ye , Modern Catalytic Methods for Organic Synthesis with Diazo Compounds , John Wiley and Sons , New York , 1998

2. Recent studies on the reactions of α-diazocarbonyl compounds

3. S. Muthusamy and J.Krishnamurthi , in Topics in Hetereocyclic Chemistry , ed. A. Hassner , Springer , 2008 , vol. 12 , pp. 147–192

4. Organic Synthesis with .alpha.-Diazo Carbonyl Compounds

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