Synthesis of diversely substituted bis-pyrrolizidino/ thiopyrrolizidino oxindolo/acenaphthyleno curcuminoids via sequential azomethine ylide cycloaddition-Reference-Cited by-同舟云学术

Synthesis of diversely substituted bis-pyrrolizidino/ thiopyrrolizidino oxindolo/acenaphthyleno curcuminoids via sequential azomethine ylide cycloaddition

Published:2018 Issue:34 Volume:8 Page:18938-18951
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Singh Meenakshi¹²³,Hazra Abhijit¹²³^ORCID,Bharitkar Yogesh P.¹²³^ORCID,Kalia Ritu¹²³,Sahoo Ashutosh⁴⁵⁶²³,Saha Sneha¹²³,Ravichandiran V.¹²³,Ghosh Shekhar⁴⁵⁶²³,Mondal Nirup B.⁴⁵⁶²³

Affiliation:

1. National Institute of Pharmaceutical Education and Research (NIPER)

2. Kolkata – 700 032

3. India

4. Department of Organic and Medicinal Chemistry

5. Indian Institute of Chemical Biology

6. Council of Scientific and Industrial Research

Abstract

Curcumin has been transformed to several diversely substituted bis-pyrrolizidino/thiopyrrolizidino oxindolo/acenaphthyleno curcuminoids via a sequential azomethine ylide cycloaddition reaction.

Funder

Department of Science and Technology, Ministry of Science and Technology

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/RA/C8RA02725K

Reference35 articles.

1. Assessment of structural diversity in combinatorial synthesis

2. Chemical genetics to chemical genomics: small molecules offer big insights