Abstract
Abstract 2,3-Disubstituted norbornenes 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.
Dates
Type | When |
---|---|
Created | 19 years, 1 month ago (July 24, 2006, 11:01 p.m.) |
Deposited | 1 year, 7 months ago (Jan. 19, 2024, 6:51 a.m.) |
Indexed | 1 year, 7 months ago (Jan. 19, 2024, 7:03 p.m.) |
Issued | 38 years, 8 months ago (Jan. 1, 1987) |
Published | 38 years, 8 months ago (Jan. 1, 1987) |
Published Online | 19 years, 5 months ago (March 27, 2006) |
Published Print | 38 years, 8 months ago (Jan. 5, 1987) |
@article{Kosugi_1987, title={Palladium Catalyzed Reactions of Organic Halides with Organotin Compounds Involving Insertion of Norbornene. Synthesis of 2,3-Disubstituted Norbornane}, volume={16}, ISSN={1348-0715}, url={http://dx.doi.org/10.1246/cl.1987.193}, DOI={10.1246/cl.1987.193}, number={1}, journal={Chemistry Letters}, publisher={Oxford University Press (OUP)}, author={Kosugi, Masanori and Tamura, Hiroyuki and Sano, Hiroshi and Migita, Toshihiko}, year={1987}, month=jan, pages={193–194} }