Literature DB >> 23926596

Domino Rh-catalyzed hydroformylation-double cyclization of o-amino cinnamyl derivatives: applications to the formal total syntheses of physostigmine and physovenine.

Wen-Hua Chiou1, Chien-Lun Kao, Jui-Chi Tsai, Yun-Man Chang.   

Abstract

A parallel, versatile and efficient route to synthesis of pyrrolidinoindoline and tetrahydrofuranoindoline alkaloids from cinnamyl derivatives has been developed, featuring a domino Rh-catalyzed hydroformylation-double cyclization sequence. This method can be applied to the syntheses of anti-Alzheimer drugs such as physostigmine and physovenine.

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Year:  2013        PMID: 23926596     DOI: 10.1039/c3cc43257b

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  A Cascade Reaction of Cinnamyl Azides with Acrylates Directly Generates Tetrahydro-Pyrrolo-Pyrazole Heterocycles.

Authors:  Angela S Carlson; En-Chih Liu; Joseph J Topczewski
Journal:  J Org Chem       Date:  2020-04-20       Impact factor: 4.354

2.  Pardon the Interruption: A Modification of Fischer's Venerable Reaction for the Synthesis of Heterocycles and Natural Products.

Authors:  Robert B Susick; Lucas A Morrill; Elias Picazo; Neil K Garg
Journal:  Synlett       Date:  2017       Impact factor: 2.454

Review 3.  Inhibitors of acetylcholinesterase and butyrylcholinesterase meet immunity.

Authors:  Miroslav Pohanka
Journal:  Int J Mol Sci       Date:  2014-06-02       Impact factor: 5.923

  3 in total

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