- Novel 1,4-palladium migration in organopalladium intermediates derived from o-lodobiaryls
-
A novel 1,4-palladium migration in organopalladium intermediates derived from o-iodobiaryls has been observed under modified Heck reaction conditions. This migration process can be switched "on" or "off" by simply choosing the appropriate reaction conditi
- Campo, Marino A.,Larock, Richard C.
-
-
Read Online
- Intramolecular Electrophilic Cyclization Approach to 6-Substituted Naphtho[2,1- b]benzofurans: Novel Dual-State Emissive Fluorophores with Blue Emission
-
A regiospecific synthesis of naphtho[2,1-b]benzofurans with a substituent at the C6 position was achieved via intramolecular 6-endo-dig electrophilic cyclization under acidic conditions to construct the central aromatic C ring. Screening of the synthesize
- Singh, Dileep Kumar,Jang, Kyungkuk,Kim, Jinhwang,Lee, Jeeyeon,Kim, Ikyon
-
p. 408 - 416
(2019/05/01)
-
- Synthesis of fluoren-9-ones by the palladium-catalyzed cyclocarbonylation of o-halobiaryls
-
The synthesis of various substituted fluoren-9-ones has been accomplished by the palladium-catalyzed cyclocarbonylation of o-halobiaryls. The cyclocarbonylation of 4′-substituted 2-iodobiphenyls produces very high yields of 2-substituted fluoren-9-ones bearing either electron-donating or electron-withdrawing substituents. 3′-Substituted 2-iodobiphenyls afford 3-substituted fluoren-9-ones in excellent yields with good regioselectivity. This chemistry has been successfully extended to polycyclic fluorenones and fluorenones containing fused isoquinoline, indole, pyrrole, thiophene, benzothiophene, and benzofuran rings.
- Campo, Marino A.,Larock, Richard C.
-
p. 5616 - 5620
(2007/10/03)
-