Literature DB >> 23683051

Synthesis of densely functionalized 3a,4-dihydro-1H-pyrrolo[1,2-b]pyrazoles via base mediated domino reaction of vinyl malononitriles with 1,2-diaza-1,3-dienes.

Orazio A Attanasi1, Gianfranco Favi, Athina Geronikaki, Fabio Mantellini, Giada Moscatelli, Aliki Paparisva.   

Abstract

A domino reaction of vinyl malononitriles (VMs) with 1,2-diaza-1,3-dienes (DDs) produce unprecedented 3a,4-dihydro-1H-pyrrolo[1,2-b]pyrazole systems in a chemo-, regio-, and stereoselective fashion. This base promoted (DIPEA) one-pot transformation involving multiple steps constructs one new C-C bond, two C-N bonds, and two new fused heterocyclic rings with total atom economy.

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Year:  2013        PMID: 23683051     DOI: 10.1021/ol401336s

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Diastereoselective synthesis of cyclohexadienes via tandem cyclization strategies.

Authors:  Abdolali Alizadeh; Akram Bagherinejad; Fahimeh Bayat; Seyed Yasub Hosseini; Long-Guan Zhu
Journal:  Mol Divers       Date:  2018-12-05       Impact factor: 2.943

2.  Catalytic Asymmetric Formal [3+2] Cycloaddition of Azoalkenes with 3-Vinylindoles: Synthesis of 2,3-Dihydropyrroles.

Authors:  Guang-Jian Mei; Wenrui Zheng; Théo P Gonçalves; Xiwen Tang; Kuo-Wei Huang; Yixin Lu
Journal:  iScience       Date:  2020-01-31
  2 in total

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