Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Louis A. Kapicak"'
Autor:
Louis S. Kapicak, Koppaka V. Rao
Publikováno v:
Journal of Heterocyclic Chemistry. 13:1073-1077
Oxidation of the alkaloids (-)tylocrebrine, (-)septicine and (±)canadine by N-bromosuccinimide gave the corresponding tetradehydroiminium salts in which the six-membered heterocyclic rings were aromatized. Evidence was provided for the preferred pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26763b579c100c01cad04debafe9ef0e
https://doi.org/10.1002/jhet.5570130527
https://doi.org/10.1002/jhet.5570130527
Publikováno v:
Tetrahedron Letters. 8:4447-4450
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::042d7af1dd0f7956e875011a1b76ffc4
https://doi.org/10.1016/s0040-4039(01)89531-9
https://doi.org/10.1016/s0040-4039(01)89531-9
Publikováno v:
Synthetic Communications. 3:311-315
The acid-catalyzed bridge cleavage reactions of 8-oxabi-cyclo [3.2.1.] octa-2,5-dienes (1) are of considerable synthetic as well as mechanistic interest since they potentially provide a direct route to aromatic tropylium systems (equation 1). We now
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c7df86b8a605f541c121d463de46b5e
https://doi.org/10.1080/00397917308065924
https://doi.org/10.1080/00397917308065924
Autor:
Louis A. Kapicak, Merle A. Battiste
Publikováno v:
Synthesis. 1971:153-154
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e98b69c03353661e4004a79189f38eda
https://doi.org/10.1055/s-1971-21688
https://doi.org/10.1055/s-1971-21688
Autor:
Louis A. Kapicak, Merle A. Battiste
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :930
Benzyne reacts with [2,2](2,5)-furanophane (1) to afford a non-internally cyclized 1:1 adduct (2) which on further reaction yields the first example, (3), of a 2:1 cycloadduct in this series.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e5d9f72c3f3835544c027029bf9eebc
https://doi.org/10.1039/c39730000930
https://doi.org/10.1039/c39730000930