ICCAS OpenIR
Highly diastereoselective synthesis of N-protected arylglycine derivatives via TiCl4-promoted Friedel-Crafts reaction of phenols with chiral N,O-hemiacetal
Ge, CS; Chen, YJ; Wang, D
2002
Source PublicationSYNLETT
ISSN0936-5214
Issue1Pages:37-42
AbstractThe 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.
KeywordFriedel-crafts Reaction Arylglycine Chiral n O-hemiacetal
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000173162300006
PublisherGEORG THIEME VERLAG KG
Citation statistics
Cited Times:17[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/79542
Collection中国科学院化学研究所
Corresponding AuthorChen, YJ
AffiliationChinese Acad Sci, Inst Chem, Ctr Mol Sci, Beijing 100080, Peoples R China
Recommended Citation
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.
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