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Search results for: ritter reaction

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... the corresponding N-tert-butyl amides: a modified Ritter reaction K. Laxma Reddy* * ... Research and Development, Bristol-Myers Squibb Pharmaceutical Research Institute, 5 Research Parkway, Wallingford ...
URL: http://www.organic-chemistry.org/abstracts/literature/610.shtm
... Temperature Shenlin Huang, Karl R. Voigtritter, John B. Unger, Bruce ... 10.1055/s-0030-1258540 see article for more reactions Abstract Taking advantage of micellar catalysis in ...
URL: http://www.organic-chemistry.org/abstracts/lit3/002.shtm
... . Krasovskiy, Stephen Haley, Karl Voigtritter and Bruce H. Lipshutz* * ... Supporting Information) see article for more reactions Abstract A new combination of reagents enables ...
URL: http://www.organic-chemistry.org/abstracts/lit4/598.shtm
... the amide group as the nitrile via retro-Ritter reaction is avoided in a modified Bischler-Napieralski ... by its conversion to an N-acyliminium intermediate with oxalyl chloride-FeCl 3. Removal of the ...
URL: http://www.organic-chemistry.org/abstracts/lit2/137.shtm
... . Huang, K. R. Voigtritter, H. B. Unger, ... for more examples see article for more reactions Asymmetric CuH-Catalyzed 1,4-Reductions in Water ...
URL: http://www.organic-chemistry.org/abstracts/literature/229.shtm
... Synthesis of Cephalostatin 1 The cephalostatins and ritterazines, represented by Cephalostatin 1 (3 ... to give the known aldehyde 5. Reaction of 5 with N-phenyltriazolenedione (6) ...
URL: http://www.organic-chemistry.org/Highlights/2010/01November.shtm
... to the unsaturated nitrile 5. Tobias Ritter of Harvard University established (Angew. ... into the allylic amine 15. This reaction is likely proceeding via an intermediate alkenyl ...
URL: http://www.organic-chemistry.org/Highlights/2016/29February.shtm
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