Organocatalytic Asymmetric Formal [3+2] Cycloaddition as a Versatile Platform to Access Methanobenzo[7]annulenes

dc.contributor.author Ramachary, Dhevalapally B.
dc.contributor.author Anif Pasha, Mohammed
dc.contributor.author Thirupathi, Guguloth
dc.date.accessioned 2022-03-27T09:38:23Z
dc.date.available 2022-03-27T09:38:23Z
dc.date.issued 2017-10-09
dc.description.abstract Pharmaceutically and structurally important methanobenzo[7]annulenes were synthesized in very good yields with excellent enantio- and diastereoselectivities through an unprecedented organocatalytic formal [3+2] cycloaddition from readily available 2-alkyl-3-hydroxynaphthalene-1,4-diones and alkyl vinyl ketones.
dc.identifier.citation Angewandte Chemie - International Edition. v.56(42)
dc.identifier.issn 14337851
dc.identifier.uri 10.1002/anie.201706557
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/anie.201706557
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13144
dc.subject cycloaddition
dc.subject heterocycles
dc.subject hydrogen bonds
dc.subject ketones
dc.subject organocatalysis
dc.title Organocatalytic Asymmetric Formal [3+2] Cycloaddition as a Versatile Platform to Access Methanobenzo[7]annulenes
dc.type Journal. Article
dspace.entity.type
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