Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Marc J. Chapdelaine"'
Autor:
Linda M. Pullan, Jeffrey M. Goldstein, James R. Damewood, Paul F. Jackson, Jeffrey A. McKinney, Timothy Davenport, Gregory G. Harris, Laura Garcia, Margaret G. Melville, Marc J. Chapdelaine
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 5:3097-3100
A series of 4-arylbenz[b]azepine analogs were prepared and shown to act as antagonists at the strychnine-insensitive glycine receptor. The heteroaryl substituted benz[b]azepine derivative 11 also showed excellent in vivo activity.
Autor:
Marc J. Chapdelaine, Martin Hulce
Publikováno v:
ChemInform. 22
Vicinal difunctionalization reactions play an important role in modern synthetic organic chemistry. They provide access to complex structures in a stereocontrolled fashion and act as powerful, attractive, convergent elements in synthetic strategy. Co
Autor:
Timothy Davenport, Paul F. Jackson, Gregory G. Harris, Laura Garcia, Jeffrey A. McKinney, James R. Damewood, Linda M. Pullan, Marc J. Chapdelaine, Margaret G. Melville, Jeffrey M. Goldstein
Publikováno v:
ChemInform. 27
A series of 4-arylbenz[b]azepine analogs were prepared and shown to act as antagonists at the strychnine-insensitive glycine receptor. The heteroaryl substituted benz[b]azepine derivative 11 also showed excellent in vivo activity.
Autor:
Marc J. Chapdelaine, Martin Hulce
Vicinal difunctionalization reactions have been extensively exploited in synthetic organic chemistry providing rapid, convergent access to complex structures in a stereocontrolled fashion. Examples of these reactions are numerous;1 classical reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::026e4acf060fd9787de13de4026b07f8
https://doi.org/10.1016/b978-0-08-052349-1.00095-0
https://doi.org/10.1016/b978-0-08-052349-1.00095-0
Autor:
Marc J. Chapdelaine, Martin Hulce
Publikováno v:
Organic Reactions
Vicinal difunctionalization reactions play an important role in modern synthetic organic chemistry. They provide access to complex structures in a stereocontrolled fashion and act as powerful, attractive, convergent elements in synthetic strategy. Co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11f2e29701abb79bdac209411e5d59ca
https://doi.org/10.1002/0471264180.or038.02
https://doi.org/10.1002/0471264180.or038.02
Publikováno v:
Tetrahedron Letters, Vol. 19, No 44 (1978) pp. 4209-4212
Autor:
Marc J. Chapdelaine, Gary H. Posner
Publikováno v:
Tetrahedron Letters. 18:3227-3230
Publikováno v:
Tetrahedron Letters, Vol. 19, No 44 (1978) pp. 4205-4208
Publikováno v:
The Journal of Organic Chemistry. 44:3661-3665
Publikováno v:
The Journal of Organic Chemistry. 54:1218-1221