70538-46-4Relevant articles and documents
Synthesis of?compounds with antiproliferative activity as?analogues of?prenylated natural products existing in?Brazilian propolis
Pisco, Laura,Kordian, Marcus,Peseke, Klaus,Feist, Holger,Michalik, Dirk,Estrada, Ernesto,Carvalho, Jo?o,Hamilton, Gerhard,Rando, Daniela,Quincoces, Jose
, p. 401 - 407 (2006)
This work describes the syntheses and antitumoral properties of five prenyl compounds from which antiproliferative activities were predicted by using the TOPS-MODE approach, a computational method for drug design. The syntheses of 2-(3-methylbut-2-enyloxy
AuCl3-Catalyzed Ring-Closing Carbonyl–Olefin Metathesis
Wang, Rui,Chen, Yi,Shu, Mao,Zhao, Wenwen,Tao, Maoling,Du, Chao,Fu, Xiaoya,Li, Ao,Lin, Zhihua
supporting information, p. 1941 - 1946 (2020/02/11)
Compared with the ripeness of olefin metathesis, exploration of the construction of carbon–carbon double bonds through the catalytic carbonyl–olefin metathesis reaction remains stagnant and has received scant attention. Herein, a highly efficient AuCl3-catalyzed intramolecular ring-closing carbonyl–olefin metathesis reaction is described. This method features easily accessible starting materials, simple operation, good functional-group tolerance and short reaction times, and provides the target cyclopentenes, polycycles, benzocarbocycles, and N-heterocycle derivatives in good to excellent yields.
Synthesis and structure elucidation of a series of chloroquinoline-2-chalcones by the Doebner–Miller reaction
Gopaul, Kaalin,Koorbanally, Neil A.
, p. 677 - 683 (2016/08/27)
-
