Regio‐ and Stereospecific Desulfinylative Chlorination of Spiroaziridine Oxindoles at Spiro‐Center for Formal [3+2]‐Cycloaddition with CS 2 : Sequential One‐Pot Synthesis of (−)‐Spirobrassinin
Author:
Affiliation:
1. Centre of Biomedical Research Sanjay Gandhi Post-Graduate Institute of Medical Sciences Campus Raebareli Road Lucknow 226014 Uttar Pradesh India
2. University of Kalyani Kalyani 741235 Nadia, West Bengal India
Funder
Science and Engineering Research Board
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202200514
Reference67 articles.
1. For selected recent reviews see:
2. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents
3. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids
4. Gelsemine: A Thought-Provoking Target for Total Synthesis
5. Total Synthesis of Complex Cyclotryptamine Alkaloids: Stereocontrolled Construction of Quaternary Carbon Stereocenters
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1. Recent advances in the accessibility, synthetic utility, and biological applications of aziridines;Organic & Biomolecular Chemistry;2023
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