LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Highly enantioselective Friedel–Crafts alkylation reaction catalyzed by rosin-derived tertiary amine–thiourea: synthesis of modified chromanes with anticancer potency
Department羰基合成与选择氧化国家重点实验室
蒋先兴; 吴立朋; 邢燕红; 王龙; 王守磊; 陈宗耀; 王锐
2012
Source PublicationChem. Commun.
ISSN1359-7345
Volume48Pages:446-448
Subject Area物理化学
Funding Organizationthe National Natural Science Foundation of China (Nos. 20932003;90813012);the Key National S&T Program “Major New Drug Development” of the Ministry of Science and Technology of China (2009ZX09503-017);the Fundamental Research Funds for the Central Universities of China (860618)
Indexed BySCI
Language英语
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/3802
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding Author王锐
Recommended Citation
GB/T 7714
蒋先兴,吴立朋,邢燕红,等. Highly enantioselective Friedel–Crafts alkylation reaction catalyzed by rosin-derived tertiary amine–thiourea: synthesis of modified chromanes with anticancer potency[J]. Chem. Commun.,2012,48:446-448.
APA 蒋先兴.,吴立朋.,邢燕红.,王龙.,王守磊.,...&王锐.(2012).Highly enantioselective Friedel–Crafts alkylation reaction catalyzed by rosin-derived tertiary amine–thiourea: synthesis of modified chromanes with anticancer potency.Chem. Commun.,48,446-448.
MLA 蒋先兴,et al."Highly enantioselective Friedel–Crafts alkylation reaction catalyzed by rosin-derived tertiary amine–thiourea: synthesis of modified chromanes with anticancer potency".Chem. Commun. 48(2012):446-448.
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