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374 related items for PubMed ID: 24375806
1. Carbocations as Lewis acid catalysts in Diels-Alder and Michael addition reactions. Bah J, Franzén J. Chemistry; 2014 Jan 20; 20(4):1066-72. PubMed ID: 24375806 [Abstract] [Full Text] [Related]
2. Enantioselective Diels-Alder reaction of anthracene by chiral tritylium catalysis. Zhang Q, Lv J, Luo S. Beilstein J Org Chem; 2019 Jan 20; 15():1304-1312. PubMed ID: 31293679 [Abstract] [Full Text] [Related]
4. (1R)-(+)-camphor and acetone derived alpha'-hydroxy enones in asymmetric Diels-Alder reaction: catalytic activation by Lewis and Brønsted acids, substrate scope, applications in syntheses, and mechanistic studies. Bañuelos P, García JM, Gómez-Bengoa E, Herrero A, Odriozola JM, Oiarbide M, Palomo C, Razkin J. J Org Chem; 2010 Mar 05; 75(5):1458-73. PubMed ID: 20121243 [Abstract] [Full Text] [Related]
8. Asymmetric Lewis acid organocatalysis of the Diels-Alder reaction by a silylated C-H acid. Gatzenmeier T, van Gemmeren M, Xie Y, Höfler D, Leutzsch M, List B. Science; 2016 Feb 26; 351(6276):949-52. PubMed ID: 26917765 [Abstract] [Full Text] [Related]
10. Metal-free, noncovalent catalysis of diels-alder reactions by neutral hydrogen bond donors in organic solvents and in water. Wittkopp A, Schreiner PR. Chemistry; 2003 Jan 20; 9(2):407-14. PubMed ID: 12532289 [Abstract] [Full Text] [Related]
12. Evidence that protons can be the active catalysts in Lewis acid mediated hetero-Michael addition reactions. Wabnitz TC, Yu JQ, Spencer JB. Chemistry; 2004 Jan 23; 10(2):484-93. PubMed ID: 14735517 [Abstract] [Full Text] [Related]
13. Structures, Lewis Acidities, Electrophilicities, and Protecting Group Abilities of Phenylfluorenylium and Tritylium Ions. Follet E, Mayer P, Berionni G. Chemistry; 2017 Jan 12; 23(3):623-630. PubMed ID: 27723164 [Abstract] [Full Text] [Related]