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Catalytic Asymmetric Aza‐Diels‐Alder Reaction: Pivotal Milestones and Recent Applications to Synthesis of Nitrogen‐Containing Heterocycles Review

Journal Advanced Synthesis & Catalysis
ISSN: 1615-4169 , E-ISSN: 1615-4150
Output data Year: 2021, Volume: 363, Number: 6, Pages: 1466-1526 Pages count : 61 DOI: 10.1002/adsc.202001307
Authors Vinogradov Maxim G. 1 , Turova Olga V. 1 , Zlotin Sergei G. 1
Affiliations
1 N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation

Abstract: In this review, the pivotal achievements and recent advances in catalytic asymmetric aza-DAR reported up to 2020 are retrospectively considered and their potency for enantioselective synthesis of useful chiral piperidine, quinoline, pyridazine, oxazine and oxadiazine derivatives and fused compounds of higher molecular complexity bearing these pharmacology-relevant heterocyclic scaffolds is demonstrated. The reported data are systematized according both to key electron transfer modes (normal or invers electron demand reactions) and to main types of attainable heterocyclic products. Of significant attention are an analysis of activation strategies (complexation, enamine or enolate formation, H-bonding, etc.) applicable to reactions with particular types of dienes and dienophiles and identification of plausible reaction pathways (either concerted or stepwise) over stereoselective cyclization processes. The review contains 310 references and 122 synthetic schemes.
Cite: Vinogradov M.G. , Turova O.V. , Zlotin S.G.
Catalytic Asymmetric Aza‐Diels‐Alder Reaction: Pivotal Milestones and Recent Applications to Synthesis of Nitrogen‐Containing Heterocycles
Advanced Synthesis & Catalysis. 2021. V.363. N6. P.1466-1526. DOI: 10.1002/adsc.202001307 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000614187800001
Scopus: 2-s2.0-85100506101
OpenAlex: W3121620969
Citing:
DB Citing
OpenAlex 59
Web of science 57
Scopus 57
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