Stereoselective synthesis of dispiroindano pyrrolidines by the [3 + 2] cycloaddition of thiazolo[3,2‐a]indole tethered dipolarophile with azomethine ylides
Author:
Affiliation:
1. Department of Chemistry University of Kerala Thiruvananthapuram Kerala India
Funder
University Grants Commission of Bangladesh
Publisher
Wiley
Subject
Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.4481
Reference22 articles.
1. A New Indanone from the Marine Cyanobacterium Lyngbya majuscula That Inhibits Hypoxia-Induced Activation of the VEGF Promoter in Hep3B Cells
2. Privileged Structures: A Useful Concept for the Rational Design of New Lead Drug Candidates
3. Identification of Fredericamycin E from Streptomyces griseus: Insights into Fredericamycin A Biosynthesis Highlighting Carbaspirocycle Formation
4. Total synthesis of coleophomone DElectronic supplementary information (ESI) available: selected physical data for compound 18. See http://www.rsc.org/suppdata/cc/b2/b208236p/
5. Diastereoselective synthesis of novel spiro indanone fused pyrano[3,2-c]chromene derivatives following hetero-Diels–Alder reaction andin vitroanticancer studies
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