An Approach to the Synthesis of Pyrimido[b]azepines via Ruthenium-Catalyzed Ring-Closing Metathesis

Abstract A highly efficient approach to the synthesis of a series of pyrimido[ b ]azepines has been developed with 5-allyl-2,4,6-trichloropyrimidine as the starting material in six or seven steps via a ring-closing metathesis (RCM) reaction. The absolute configuration of the key intermediate pyrimid...

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Veröffentlicht in:Synthesis (Stuttgart) 2015-11, Vol.47 (21), p.3292-3300
Hauptverfasser: Zhang, Tong-Bo, Yang, Quan-Zhi, Cao, Yuan-Yuan, Wu, Shao-Tong, Zhang, Yu, Guo, Ying, Zhao, Jian-Xiong, Sun, Xue-Feng, Zhang, Zhi-Li, Tian, Chao, Liu, Jun-Yi, Wang, Xiao-Wei
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container_end_page 3300
container_issue 21
container_start_page 3292
container_title Synthesis (Stuttgart)
container_volume 47
creator Zhang, Tong-Bo
Yang, Quan-Zhi
Cao, Yuan-Yuan
Wu, Shao-Tong
Zhang, Yu
Guo, Ying
Zhao, Jian-Xiong
Sun, Xue-Feng
Zhang, Zhi-Li
Tian, Chao
Liu, Jun-Yi
Wang, Xiao-Wei
description Abstract A highly efficient approach to the synthesis of a series of pyrimido[ b ]azepines has been developed with 5-allyl-2,4,6-trichloropyrimidine as the starting material in six or seven steps via a ring-closing metathesis (RCM) reaction. The absolute configuration of the key intermediate pyrimido[4,5- b ]azepine was ascertained by X-ray crystal structure analysis.
doi_str_mv 10.1055/s-0034-1381009
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title An Approach to the Synthesis of Pyrimido[b]azepines via Ruthenium-Catalyzed Ring-Closing Metathesis
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