Preparation of Substituted Pyrimido[4,5-b]-1,4-benzoxazepines, Thiazepines, and Diazepines via a Pictet−Spengler Cyclization

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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Veröffentlicht in:Journal of organic chemistry 2005-11, Vol.70 (23), p.9629-9631
Hauptverfasser: Duncton, Matthew A. J, Smith, Leon M, Burdzovic-Wizeman, Sabina, Burns, Aaron, Liu, Hu, Mao, Yunyu, Wong, Wai C, Kiselyov, Alexander S
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container_end_page 9631
container_issue 23
container_start_page 9629
container_title Journal of organic chemistry
container_volume 70
creator Duncton, Matthew A. J
Smith, Leon M
Burdzovic-Wizeman, Sabina
Burns, Aaron
Liu, Hu
Mao, Yunyu
Wong, Wai C
Kiselyov, Alexander S
description 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.
doi_str_mv 10.1021/jo051419g
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source MEDLINE; American Chemical Society Journals
subjects Azepines - chemical synthesis
Azepines - chemistry
Catalysis
Chemistry
Cyclization
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
Molecular Structure
Organic chemistry
Preparations and properties
title Preparation of Substituted Pyrimido[4,5-b]-1,4-benzoxazepines, Thiazepines, and Diazepines via a Pictet−Spengler Cyclization
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