中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly diastereoselective synthesis of N-protected arylglycine derivatives via TiCl4-promoted Friedel-Crafts reaction of phenols with chiral N,O-hemiacetal

文献类型:期刊论文

作者Ge, CS; Chen, YJ; Wang, D
刊名SYNLETT
出版日期2002
期号1页码:37-42
关键词Friedel-crafts Reaction Arylglycine Chiral n O-hemiacetal
ISSN号0936-5214
英文摘要The optically active N-protected arylglycine derivatives were obtained via TiCl4-promoted Friedel-Crafts reaction of various phenols with chiral N,O-hemiacetals in excellent diastereoselectivity.
语种英语
WOS记录号WOS:000173162300006
出版者GEORG THIEME VERLAG KG
源URL[http://ir.iccas.ac.cn/handle/121111/79541]  
专题中国科学院化学研究所
通讯作者Chen, YJ
作者单位Chinese Acad Sci, Inst Chem, Ctr Mol Sci, Beijing 100080, Peoples R China
推荐引用方式
GB/T 7714
Ge, CS,Chen, YJ,Wang, D. Highly diastereoselective synthesis of N-protected arylglycine derivatives via TiCl4-promoted Friedel-Crafts reaction of phenols with chiral N,O-hemiacetal[J]. SYNLETT,2002(1):37-42.
APA Ge, CS,Chen, YJ,&Wang, D.(2002).Highly diastereoselective synthesis of N-protected arylglycine derivatives via TiCl4-promoted Friedel-Crafts reaction of phenols with chiral N,O-hemiacetal.SYNLETT(1),37-42.
MLA Ge, CS,et al."Highly diastereoselective synthesis of N-protected arylglycine derivatives via TiCl4-promoted Friedel-Crafts reaction of phenols with chiral N,O-hemiacetal".SYNLETT .1(2002):37-42.

入库方式: OAI收割

来源:化学研究所

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