Selective synthesis of multiply substituted 7-norbornenone derivatives or Diels–Alder cycloadducts from 1,2,3,4-tetrasubstituted 1,3-butadienes and maleic anhydride with or without Lewis acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference61 articles.
1. Lewis Acid Promoted Tandem Intermolecular Diels−Alder/Intramolecular Allylation Reactions of Silyl-Substituted 1,3-Butadienes Leading to Multisubstituted 7-Norbornenones and Related Polycyclic Compounds
2. Modulation of π-facial selectivities in nucleophilic additions to 7-norbornenones
3. Ground state geometric distortions distal substituent effects in determining the β-facial selectivity in 7-norbornenones
4. π-Facial selectivities in nucleophilic additions to 4-hetero-tricyclo[5.2.1.02,6]decan-10-ones and 4-hetero-tricyclo[5.2.1.02,6]dec-8-en-10-ones: an experimental and computational study
5. Development of predictive models of π-facial selectivity; a critical study of nucleophilic addition to sterically unbiased ketones
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