Development of Tartaric Acid Derived Hydrogen-Bond Donors

被引：7
作者：
Lauber, Markus Boris [1 ]
Froehlich, Roland [2 ]
Paradies, Jan [1 ]
机构：
[1] Karlsruhe Inst Technol, Inst Organ Chem, D-76131 Karlsruhe, Germany
[2] Univ Munster, Inst Organ Chem, D-48149 Munster, Germany
来源：
SYNTHESIS-STUTTGART | 2012年 / 44卷 / 20期
关键词：
TADDOL; thiourea; hydrogen bond; asymmetric synthesis; catalyst; BAYLIS-HILLMAN REACTION; DIELS-ALDER REACTIONS; CYCLIC MESO-ANHYDRIDES; ISOPROPYL HEMIESTERS; ASYMMETRIC CATALYSIS; METAL-FREE; TADDOL; ORGANOCATALYST; DERIVATIVES; ACTIVATION;
D O I：
10.1055/s-0032-1316759
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A flexible synthesis of bifunctional thiourea derivatives based on the TADDOL framework is described. Hydroxy as well as primary, secondary, and tertiary amino-substituted bifunctional hydrogen-bond donors were synthesized.
引用
收藏
页码：3209 / 3215
页数：7
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