Organic Chemistry Portal
Reactions >> Related Literature


Search results for: prins reaction

8 results found containing all search terms.
... mechanism Key Words Tetrahydropyrans, Prins Reaction ID: J54-Y2007-1910 ... mild conditions. A plausible Prins-type reaction mechanism has been ... . see article for more examples proposed mechanism Key Words ...
URL: http://www.organic-chemistry.org/abstracts/lit1/734.shtm
... Organic Chemistry Portal Selective Prins Reaction of Styrenes and Formaldehyde Catalyzed by 2, ... (difluoro)borane Thorsten Bach*, Johannes Löbel *Technische Universität München, ...
URL: http://www.organic-chemistry.org/abstracts/literature/185.shtm
... successfully employed as a reaction medium for Prins cyclizations, to produce 4-chlorotetrahydropyran derivatives in ... Lewis Acidic Chloroaluminate Ionic Liquids: Novel Reaction Media for the Synthesis of 4-Chloropyrans Jhillu ...
URL: http://www.organic-chemistry.org/abstracts/literature/535.shtm
... Organic Chemistry Portal Highly Stereoselective Prins Cyclization of (Z)- and ( ... proposed mechanism Key Words Tetrahydropyrans, Prins Reaction, 1,2-Dibromoalkanes ID: J54-Y2007-1620 ...
URL: http://www.organic-chemistry.org/abstracts/lit1/702.shtm
... of the starting epoxide 8. The Prins cyclization has become a workhorse of six-membered ... He included a trapping aldehyde in the reaction mixture, and found that product ee ...
URL: http://www.organic-chemistry.org/Highlights/2006/10April.shtm
... Peroxide Myriam Mba, Leonard J. Prins and Giulia Licini* *Università di ... -symmetric triphenolate amine ligand efficiently catalyzes sulfoxidation reactions at room temperature without previous activation using ...
URL: http://www.organic-chemistry.org/abstracts/lit1/545.shtm
... , 2003, 1779-1783. Key Words Prins reaction, niobium(V) chloride ... Lewis Acidic Chloroaluminate Ionic Liquids: Novel Reaction Media for the Synthesis of 4-Chloropyrans J ...
URL: http://www.organic-chemistry.org/abstracts/literature/396.shtm
... of Seoul National University, was the Prins-pinacol rearrangement of 1 to 2. Remarkably ... chiral ether of 4. The key reaction was the selective opening at the distal ...
URL: http://www.organic-chemistry.org/Highlights/2007/26November.shtm