Crossref journal-article
Oxford University Press (OUP)
Chemistry Letters (286)
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.

Bibliography

Kosugi, M., Tamura, H., Sano, H., & Migita, T. (1987). Palladium Catalyzed Reactions of Organic Halides with Organotin Compounds Involving Insertion of Norbornene. Synthesis of 2,3-Disubstituted Norbornane. Chemistry Letters, 16(1), 193–194.

Authors 4
  1. Masanori Kosugi (first)
  2. Hiroyuki Tamura (additional)
  3. Hiroshi Sano (additional)
  4. Toshihiko Migita (additional)
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)
Funders 0

None

@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} }