109324-05-2Relevant articles and documents
PALLADIUM-CATALYZED REACTION OF ORGANIC HALIDES WITH ORGANOTIN COMPOUNDS INVOLVING OLEFIN INSERTION: SYNTHESIS OF 2,3-DISUBSTITUED NORBORNANES
Kosugi, Masanori,Tamura, Hiroyuki,Sano, Hiroshi,Migita, Toshihiko
, p. 961 - 968 (2007/10/02)
2,3-Disubstituted norbornanes were prepared by the palladium-catalyzed reaction of a ternary system composed of organic halide, organotin compound, and norbornene.The scope and limitations of this reaction are described.
Palladium Catalyzed Reactions of Organic Halides with Organotin Compounds Involving Insertion of Norbornene. Synthesis of 2,3-Disubstituted Norbornane
Kosugi, Masanori,Tamura, Hiroyuki,Sano, Hiroshi,Migita, Toshihiko
, p. 193 - 194 (2007/10/02)
2,3-Disubstituted norbornanes were prepared by the palladium catalyzed reaction of a ternary system composed of organic halide, organotin compound, and norbornene.Aryl and vinyl bromides, and acyl chloride were good substrates, but benzyl and allyl chlorides were not.Vinyl, phenyl, ethynyl, and allyltin compounds were utilizable reagents.