Chiral ligands derived from abrine. Part 6: Importance of a bulky N-alkyl group in indole-containing chiral beta-tertiary amino alcohols for controlling enantioselectivity in addition of diethylzinc toward aldehydes

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	Chiral ligands derived from abrine. Part 6: Importance of a bulky N-alkyl group in indole-containing chiral beta-tertiary amino alcohols for controlling enantioselectivity in addition of diethylzinc toward aldehydes
	Dai, WM ; Zhu, HJ ; Hao, XJ
刊名	TETRAHEDRON-ASYMMETRY
	2000-06-16
卷号	11 期号:11 页码:2315-2337
关键词	Asymmetric Autocatalytic Reaction Aromatic-aldehydes Dialkylzinc Reagents Organozinc Reagents Enantiomeric Excess Organometallic Reagents Ephedrine Derivatives Aliphatic-aldehydes Aryl Aldehydes Catalysts
ISSN号	0957-4166
文献子类	Review
英文摘要	A number of chiral beta-amino alcohols possessing a 3-indolylmethyl group have been synthesized from the alkaloid (S)-abrine and elucidated for potency in the catalytic enantioselective ethylation of PhCHO with Et2Zn. In general, the secondary amines 15a-d bearing a dialkylhydroxymethyl group induced (R)-1-phenyl-1-propanol, whereas 15e-g and 18 bearing a diarylhydroxymethyl group favored the (S)-enantiomer. In contrast, the beta-tertiary amino alcohols 20b d and 21 produced (R)-1-phenyl-1-propanol. regardless of the substituents at the carbon bearing the hydroxy group. Enantiomeric excess of 87.5% was obtained for (R)-1-phenyl-1-propanol using ligand 21 as the promoter. Eleven substituted benzaldehydes and naphth-aldehydes were examined for enantioselective ethylation by using 21 and the chiral alcohols were obtained in 93-97% ee, except for o-BrC6H4CHO and p-Me2NC6H4CHO. Excellent enantioselectivity was also observed in the ethylation of cyclohexanecarboxaldehyde (94.8% ee) and 2-thiophenecarboxaldehyde (94.9% ee) by using catalytic 21. The anti 5/4/4-fused tricyclic TS I was proposed to rationalize the asymmetric induction. The diethylhydroxymethyl and N-2-t-butylethyl groups are believed to enforce the preference for the anti-TS(R) I and it results in high enantioselectivity. (C) 2000 Elsevier Science Ltd. All rights reserved.
学科主题	Chemistry, Inorganic & Nuclear ; Chemistry, Organic ; Chemistry, Physical
WOS关键词	ASYMMETRIC AUTOCATALYTIC REACTION ; AROMATIC-ALDEHYDES ; DIALKYLZINC REAGENTS ; ORGANOZINC REAGENTS ; ENANTIOMERIC EXCESS ; ORGANOMETALLIC REAGENTS ; EPHEDRINE DERIVATIVES ; ALIPHATIC-ALDEHYDES ; ARYL ALDEHYDES ; CATALYSTS
WOS研究方向	Chemistry
语种	英语
WOS记录号	WOS:000087888600011
公开日期	2012-03-21
内容类型	期刊论文
源URL	[http://ir.kib.ac.cn:8080/handle/151853/4350]
专题	昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室
作者单位	1.Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Hong Kong, Peoples R China 2.Chinese Acad Sci, Kunming Inst Bot, Kunming 650204, Yunnan, Peoples R China
推荐引用方式 GB/T 7714	Dai, WM,Zhu, HJ,Hao, XJ. Chiral ligands derived from abrine. Part 6: Importance of a bulky N-alkyl group in indole-containing chiral beta-tertiary amino alcohols for controlling enantioselectivity in addition of diethylzinc toward aldehydes[J]. TETRAHEDRON-ASYMMETRY,2000,11(11):2315-2337.
APA	Dai, WM,Zhu, HJ,&Hao, XJ.(2000).Chiral ligands derived from abrine. Part 6: Importance of a bulky N-alkyl group in indole-containing chiral beta-tertiary amino alcohols for controlling enantioselectivity in addition of diethylzinc toward aldehydes.TETRAHEDRON-ASYMMETRY,11(11),2315-2337.
MLA	Dai, WM,et al."Chiral ligands derived from abrine. Part 6: Importance of a bulky N-alkyl group in indole-containing chiral beta-tertiary amino alcohols for controlling enantioselectivity in addition of diethylzinc toward aldehydes".TETRAHEDRON-ASYMMETRY 11.11(2000):2315-2337.