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Stereospecific Decarboxylative Benzylation of Enolates: Development and Mechanistic Insight

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成果类型:
期刊论文
作者:
Li, Tian-Ren;Maliszewski, Mary L.;Xiao, Wen-Jing;Tunge, Jon A.*
通讯作者:
Tunge, Jon A.
作者机构:
[Li, Tian-Ren; Tunge, Jon A.; Maliszewski, Mary L.] Univ Kansas, Dept Chem, 2010 Malott Hall,1251 Wescoe Hall Dr, Lawrence, KS 66045 USA.
[Li, Tian-Ren; Tunge, Jon A.; Maliszewski, Mary L.] KU Chem Methodol & Lib Dev Ctr Excellence, 2034 Becker Dr, Lawrence, KS 66047 USA.
[Li, Tian-Ren; Xiao, Wen-Jing] Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China.
通讯机构:
[Tunge, Jon A.] U
[Tunge, Jon A.] K
Univ Kansas, Dept Chem, 2010 Malott Hall,1251 Wescoe Hall Dr, Lawrence, KS 66045 USA.
KU Chem Methodol & Lib Dev Ctr Excellence, 2034 Becker Dr, Lawrence, KS 66047 USA.
语种:
英文
期刊:
Organic Letters
ISSN:
1523-7060
年:
2018
卷:
20
期:
7
页码:
1730-1734
基金类别:
National Science FoundationNational Science Foundation (NSF) [CHE-1465172]; Kansas Bioscience Authority Rising Star program; China Scholarship Council (CSC)China Scholarship Council [201606770032]; NIHUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USA [S10RR024664]; NSFNational Science Foundation (NSF) [1625923]; NATIONAL CENTER FOR RESEARCH RESOURCESUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Center for Research Resources (NCRR) [S10RR024664] Funding Source: NIH RePORTER; Direct For Mathematical & Physical ScienNational Science Foundation (NSF)NSF - Directorate for Mathematical & Physical Sciences (MPS) [1465172] Funding Source: National Science Foundation; Division Of ChemistryNational Science Foundation (NSF)NSF - Directorate for Mathematical & Physical Sciences (MPS) [1465172] Funding Source: National Science Foundation
机构署名:
本校为其他机构
院系归属:
化学学院
摘要:
A palladium-catalyzed decarboxylative coupling of enol carbonates with diarylmethyl electrophiles that are derived from secondary benzylic alcohols has been developed. This method allows the generation of a variety of β-diaryl ketones through an efficient and highly stereospecific coupling. In addition, detailed mechanistic insight into the coupling suggests that the reaction is a rare example of an intramolecular decarboxylative coupling ...

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