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Pure Appl. Chem., 2005, Vol. 77, No. 12, pp. 2105-2110

http://dx.doi.org/10.1351/pac200577122105

Chiral phosphine Lewis bases in catalytic, asymmetric aza-Morita-Baylis-Hillman reaction

Min Shi and Lian-Hui Chen

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China

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  • Lee Richmond, Zhong Fangrui, Zheng Bin, Meng Yuezhong, Lu Yixin, Huang Kuo-Wei: The origin of enantioselectivity in the l-threonine-derived phosphine–sulfonamide catalyzed aza-Morita–Baylis–Hillman reaction: effects of the intramolecular hydrogen bonding. Org. Biomol. Chem. 2013, 11, 4818. <http://dx.doi.org/10.1039/c3ob40144h>
  • Garnier Jean-Marc, Anstiss Christopher, Liu Fei: Enantioselective Trifunctional Organocatalysts for Rate- Enhanced Aza-Morita-Baylis-Hillman Reactions at Room Temperature. Adv. Synth. Catal. 2009, 351, 331. <http://dx.doi.org/10.1002/adsc.200800679>
  • Denmark Scott E., Beutner Gregory L.: Lewis-Base-Katalyse in der organischen Synthese. Angew Chem 2008, 120, 1584. <http://dx.doi.org/10.1002/ange.200604943>
  • Denmark Scott E., Beutner Gregory L.: Lewis Base Catalysis in Organic Synthesis. Angew Chem Int Ed 2008, 47, 1560. <http://dx.doi.org/10.1002/anie.200604943>
  • Meng Xiangtai, Huang You, Chen Ruyu: A Novel Selective Aza-Morita-Baylis-Hillman (aza-MBH) Domino Reaction and Aza-MBH Reaction of N-Sulfonated Imines with Acrolein Catalyzed by a Bifunctional Phosphine Organocatalyst. Chem Eur J 2008, 14, 6852. <http://dx.doi.org/10.1002/chem.200800753>
  • Tang Xiaofang, Zhang Bo, He Zhengrong, Gao Ruili, He Zhengjie: 1,3,5-Triaza-7-phosphaadamantane (PTA): A Practical and Versatile Nucleophilic Phosphine Organocatalyst. Adv Synth Catal 2007, 349, 2007. <http://dx.doi.org/10.1002/adsc.200700071>
  • Rastogi Namrata, Mohan Renu, Panda Dulal, Mobin Shaikh M., Namboothiri Irishi N. N.: Synthesis and anticancer activity studies of ?-aminoalkylated conjugated nitroalkenes. Org Biomol Chem 2006, 4, 3211. <http://dx.doi.org/10.1039/b607537a>