Literature DB >> 16268648

Preparation of substituted pyrimido[4,5-b]-1,4-benzoxazepines, thiazepines, and diazepines via a Pictet-Spengler cyclization.

Matthew A J Duncton1, Leon M Smith, Sabina Burdzovic-Wizeman, Aaron Burns, Hu Liu, Yunyu Mao, Wai C Wong, Alexander S Kiselyov.   

Abstract

[Reaction: see text]. A synthesis of the title compounds, which have found use as inhibitors of certain receptor tyrosine kinases, was achieved using a Pictet-Spengler cyclization as a key step.

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Year:  2005        PMID: 16268648     DOI: 10.1021/jo051419g

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  One-pot tandem Ugi-4CR/S(N)Ar approach to highly functionalized quino[2,3-b][1,5]benzoxazepines.

Authors:  Mehdi Ghandi; Nahid Zarezadeh; Alireza Abbasi
Journal:  Mol Divers       Date:  2015-12-24       Impact factor: 2.943

Review 2.  Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid.

Authors:  Elida N Thobokholt; Enrique L Larghi; Andrea B J Bracca; Teodoro S Kaufman
Journal:  RSC Adv       Date:  2020-05-19       Impact factor: 4.036

  2 in total

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