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
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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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