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... Organic Chemistry Portal Visible-Light Induced Radical Addition-Elimination Reaction for Constructing Allylic Sulfones from Sulfonyl Chlorides and Allyl Bromides Rui-Xue Li, Yuan Chen, Lan-Qian Huang, Zhi Guan ...
... from Utah State University, USA, have demonstrated that a large number of conventional reactions commonly employed for the synthesis and/or functionalization of carbohydrates may be performed ...
... Organic Chemistry Portal Reaction of Aldehydes/Ketones with Electron-Deficient 1,3 ,5-Triazines Leading to Functionalized Pyrimidines as Diels-Alder/Retro-Diels-Alder Reaction Products: Reaction Development and ...
... Res. 2002, 35, 533. DOI: 10.1021/ar0100125; Organic Reactions in Aqueous Media, 1997, John Wiley & Sons; Org. Process ...
... Organic Chemistry Portal Exploring Phthalimide as the Acid Component in the Passerini Reaction Jingyao Li, Qiang Zheng, Alexander Dömling* *Czech Advanced Technology and Research Institute ...
... Organic Chemistry Portal Enantioselective Synthesis of Quaternary Oxindoles: Desymmetrizing Staudinger-Aza-Wittig Reaction Enabled by a Bespoke HypPhos Oxide Catalyst Changmin Xie, Jacob Kim, Binh Khanh Mai, ...
... Organic Chemistry Portal Controlling Reactivity and Selectivity in the Mizoroki-Heck Reaction: High Throughput Evaluation of 1,5-Diaza-3,7-diphosphacyclooctane Ligands Eric S. Isbrandt, Devon E ...
... Appl. Chem., 1998, 70, 1019. Key Words: DIELS-ALDER REACTIONS/SINGLE CHIRAL SOURCE/STEREOSELECTIVE SYNTHESIS/ACHIRAL LIGANDS/TRIFLUOROMETHANESULFONATES/ENANTIOMERS ...
... Organic Chemistry Portal Multicomponent Reactions Tuesday, May 5, 2005 Alexander Doemling Toluenesulphonylmethyl isocyanide (TOSMIC) and the van Leusen MCR The Chemistry of TOSMIC The chemistry ...
... addition of the aldehyde and ligand and further microwave heating for 5 min. The reaction time can be reduced from 1 day conventionally to only 15 min under microwave ...
