ICCAS OpenIR
Efficient Synthesis of Benzimidazo[1,2-a]pyrimidinone Derivatives via Catalyst-Free Reactions of Baylis-Hillman Acetates, Alcohols, and Amines with 2-Aminobenzimidazole
Wang, Yan1; Shafiq, Zahid1,2; Liu, Li1; Wang, Dong1; Chen, Yong-Jun1
2010-03-01
Source PublicationJOURNAL OF HETEROCYCLIC CHEMISTRY
ISSN0022-152X
Volume47Issue:2Pages:373-378
AbstractBenzimidazo[1,2-a]pyrimidinone and its derivatives were easily prepared in good to excellent yields via tandem reactions of 2-aminobenzimidazole with Baylis-Hillman acetates, alcohols, and amines without the use of catalyst and additive in one-pot process. The method provided an efficient and facile route to the title fused heterocyclic compounds with different functional groups.
DOI10.1002/jhet.324
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000276427300019
PublisherWILEY-BLACKWELL
Citation statistics
Cited Times:6[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/69786
Collection中国科学院化学研究所
Corresponding AuthorLiu, Li
Affiliation1.Chinese Acad Sci, Inst Chem, Beijing Natl Lab BNLMS, CAS Key Lab Mol Recognit, Beijing 100080, Peoples R China
2.BZ Univ, Dept Chem, Multan 60800, Pakistan
Recommended Citation
GB/T 7714
Wang, Yan,Shafiq, Zahid,Liu, Li,et al. Efficient Synthesis of Benzimidazo[1,2-a]pyrimidinone Derivatives via Catalyst-Free Reactions of Baylis-Hillman Acetates, Alcohols, and Amines with 2-Aminobenzimidazole[J]. JOURNAL OF HETEROCYCLIC CHEMISTRY,2010,47(2):373-378.
APA Wang, Yan,Shafiq, Zahid,Liu, Li,Wang, Dong,&Chen, Yong-Jun.(2010).Efficient Synthesis of Benzimidazo[1,2-a]pyrimidinone Derivatives via Catalyst-Free Reactions of Baylis-Hillman Acetates, Alcohols, and Amines with 2-Aminobenzimidazole.JOURNAL OF HETEROCYCLIC CHEMISTRY,47(2),373-378.
MLA Wang, Yan,et al."Efficient Synthesis of Benzimidazo[1,2-a]pyrimidinone Derivatives via Catalyst-Free Reactions of Baylis-Hillman Acetates, Alcohols, and Amines with 2-Aminobenzimidazole".JOURNAL OF HETEROCYCLIC CHEMISTRY 47.2(2010):373-378.
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