LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Asymmetric addition of benzothiazole to N-tert-butanesulfinyl imine for the synthesis of chiral a-branched heteroaryl amines
Department羰基合成与选择氧化国家重点实验室
Zhang JL(张金龙); Yang YH(杨玉红); Wang M(王梅); Lin L(林利); Wang R(王锐)
2012
Source PublicationTetrahedron Letters
ISSN0040-4039
Volume53Pages:6893-6896
AbstractThis work concerns the asymmetric additions of benzothiazole to a variety of N-tert-butanesulfinyl imines with excellent diastereoselectivities (d.r. up to >99:1). Amino alkoxyl lithium was the key additive to obtain the excellent diastereoselectivity. More functionalized 4-methyl-5-vinyl thiazole and alkyl imines which can isomerize to enamines are also compatible substrates to the present protocol.
KeywordAsymmetric Synthesis Benzothiazole Diarylmethylamine Diastereoselectivity N-tert-butanesulfinyl Imine
Subject Area物理化学
Funding OrganizationNSFC (nos. 21002043;21272107;20932003);the National S&T Major Project of China (2012ZX09504-001-003);Fundamental Research Funds for the Central Universities (lzujbky-2010-184)
Indexed BySCI
Language英语
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/3882
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorLin L(林利); Wang R(王锐)
Recommended Citation
GB/T 7714
Zhang JL,Yang YH,Wang M,et al. Asymmetric addition of benzothiazole to N-tert-butanesulfinyl imine for the synthesis of chiral a-branched heteroaryl amines[J]. Tetrahedron Letters,2012,53:6893-6896.
APA 张金龙,杨玉红,王梅,林利,&王锐.(2012).Asymmetric addition of benzothiazole to N-tert-butanesulfinyl imine for the synthesis of chiral a-branched heteroaryl amines.Tetrahedron Letters,53,6893-6896.
MLA 张金龙,et al."Asymmetric addition of benzothiazole to N-tert-butanesulfinyl imine for the synthesis of chiral a-branched heteroaryl amines".Tetrahedron Letters 53(2012):6893-6896.
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