LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Highly Enantioselective Addition of Terminal Alkynes to Aldehydes Catalyzed by a New Chiral beta-Sulfonamide Alcohol/Ti((OPr)-Pr-i)(4)/Et2Zn/R3N Catalyst System
Department羰基合成与选择氧化国家重点实验室
Qiu L(邱立); Wang Q(王全); Lin L(林利); Liu XD(刘晓东); Jiang XX(蒋先兴); Zhao QY(赵庆阳); Hu GW(胡国文); Wang R(王锐)
2009
Source PublicationChirality
ISSN0899-0042
Volume21Pages:316-323
AbstractA new catalytic system, generated from the readily available and inexpensive b-sulfonamide alcohol L*, Ti(OiPr)4, Et2Zn, and tertiary amine base (R3N), effectively catalyzes the enantioselective addition of various terminal alkynes including some quite challenging alkynes to aldehydes in good yields and excellent enantioselectivities. Up to 96% yield and >99% enantioselectivity were achieved with the use of N,Ndiisoproylethylamine (DIPEA) as an additive in this asymmetric addition.
KeywordEnantioselective Addition Sulfonamide Alcohol Tertiary Amine Base Terminal Alkynes Aldehydes
Subject Area物理化学
Funding OrganizationNatural Science Foundation of China (Contract grant numbers: 20525206;20772052;20621091);Ministry of Education of China (Chang Jiang Program)
Indexed BySCI
Language英语
Citation statistics
Cited Times:25[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/572
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorWang R(王锐)
Recommended Citation
GB/T 7714
Qiu L,Wang Q,Lin L,et al. Highly Enantioselective Addition of Terminal Alkynes to Aldehydes Catalyzed by a New Chiral beta-Sulfonamide Alcohol/Ti((OPr)-Pr-i)(4)/Et2Zn/R3N Catalyst System[J]. Chirality,2009,21:316-323.
APA 邱立.,王全.,林利.,刘晓东.,蒋先兴.,...&王锐.(2009).Highly Enantioselective Addition of Terminal Alkynes to Aldehydes Catalyzed by a New Chiral beta-Sulfonamide Alcohol/Ti((OPr)-Pr-i)(4)/Et2Zn/R3N Catalyst System.Chirality,21,316-323.
MLA 邱立,et al."Highly Enantioselective Addition of Terminal Alkynes to Aldehydes Catalyzed by a New Chiral beta-Sulfonamide Alcohol/Ti((OPr)-Pr-i)(4)/Et2Zn/R3N Catalyst System".Chirality 21(2009):316-323.
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