748770-65-2Relevant articles and documents
Rhodium-catalyzed intramolecular hydroacylation of 5- and 6-alkynals: Convenient synthesis of α-alkylidenecycloalkanones and cycloalkenones
Takeishi, Kenzo,Sugishima, Koudai,Sasaki, Kaori,Tanaka, Ken
, p. 5681 - 5688 (2004)
A novel intramolecular hydroacylation of 5- and 6-alkynals leading to α-alkylidenecycloalkanones was accomplished by using cationic a rhodium(I)/BINAP complex. For all cyclizations described, a single (E)-olefin isomer was obtained. At elevated temperature, hydroacylation and double bond migration of 5- and 6-alkynals proceeded in a one-pot reaction to give cycloalkenones. An intramolecular hydroacylation of a 7-alkynal was unsuccessful. This method represents an attractive new route to highly functionalized α-alkylidenecycloalkanones and cycloalkenones.
Ligand-, copper-, and amine-free sonogashira reaction of aryl iodides and bromides with terminal alkynes
Urgaonkar, Sameer,Verkade, John G.
, p. 5752 - 5755 (2007/10/03)
Conditions for an efficient ligand-, copper-, and amine-free palladium-catalyzed Sonogashira reaction of aryl iodides and bromides with terminal alkynes have been developed. Critical to the success of this new protocol is the use of tetrabutylammonium ace