Diversity-oriented approach to intricate bis-armed spirocycles involving a two directional [2+2+2] co-trimerization and the [4+2] cycloaddition reaction as key steps
Author:
Funder
DST-New Delhi
IRCC
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference45 articles.
1. Expedient Synthesis of C3-Symmetric Hexasubstituted Benzenes via Nicholas Reaction/[2 + 2 + 2] Cycloaddition. New Platforms for Molecular Recognition
2. Constrained phenylalanyl peptides via a [2+2+2]-cycloaddition strategy
3. Synthesis of constrained phenylalanine derivatives via a [2+2+2] cycloaddition strategy
4. A new synthetic approach to 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) derivatives via a [2+2+2] cycloaddition reaction
5. Cycloaddition approach to benzo-annulated indane-based α-amino acid derivatives
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