ICCAS OpenIR
Sharpless asymmetric epoxidation of heptenylphenylmethylsilanol
Feng, WC; Wang, D
1995-08-01
Source PublicationCHINESE CHEMICAL LETTERS
ISSN1001-8417
Volume6Issue:8Pages:647-650
AbstractThe Sharpless asymmetric epoxidation of 1 was carried out to give the (1S,2S)-4 in 33% yield, which was protodesilylated giving (-)-5 with 50% ee. The steric effect of phenyl group on silicon upon the rate and ee of the reaction was observed. The possibility of kinetic resolution of racemic silanol under the Sharpless reaction condition was examined.
Indexed BySCI
Language英语
WOS IDWOS:000169109300002
PublisherCHINESE CHEMICAL SOCIETY
Citation statistics
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/74012
Collection中国科学院化学研究所
AffiliationAcad Sinica, Inst Chem, Beijing 100080, Peoples R China
Recommended Citation
GB/T 7714
Feng, WC,Wang, D. Sharpless asymmetric epoxidation of heptenylphenylmethylsilanol[J]. CHINESE CHEMICAL LETTERS,1995,6(8):647-650.
APA Feng, WC,&Wang, D.(1995).Sharpless asymmetric epoxidation of heptenylphenylmethylsilanol.CHINESE CHEMICAL LETTERS,6(8),647-650.
MLA Feng, WC,et al."Sharpless asymmetric epoxidation of heptenylphenylmethylsilanol".CHINESE CHEMICAL LETTERS 6.8(1995):647-650.
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