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Merck
CN
  • Quinine-thiourea catalyzed enantioselective hydrophosphonylation of trifluoromethyl 2(1H)-quinazolinones.

Quinine-thiourea catalyzed enantioselective hydrophosphonylation of trifluoromethyl 2(1H)-quinazolinones.

Chemical communications (Cambridge, England) (2012-12-19)
Hexin Xie, Aiguo Song, Xinshuai Zhang, Xiaobei Chen, Hao Li, Chunquan Sheng, Wei Wang
摘要

An organocatalytic enantioselective addition reaction of cyclic ketoimines with phosphites has been developed for the first time. The process, catalyzed by Soós' quinine thiourea, affords synthetically and medicinally interesting enantioenriched trifluoromethyl dihydroquinazolinones in high yields and with high enantioselectivities.

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Sigma-Aldrich
奎宁, suitable for fluorescence, anhydrous, ≥98.0% (dried material, NT)
Supelco
奎宁, certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland