Author/Authors :
Chuang، نويسنده , , Da-Wei and El-Shazly، نويسنده , , Mohamed and Chen، نويسنده , , Chin-Chau and Chung، نويسنده , , Yu-Ming and D. Barve، نويسنده , , Balaji and Wu، نويسنده , , Ming-Jung and Chang، نويسنده , , Fang-Rong and Wu، نويسنده , , Yang-Chang، نويسنده ,
Abstract :
1,5-Diphenylpent-3-en-1-yne derivatives were isolated in minor quantities from terrestrial plants and exhibited strong anti-inflammatory activity. A cross coupling reaction between B-benzyl-9-BBN and chloroenynes under mild condition was developed resulting in the formation of different 1,5-diphenylpent-3-en-1-yne derivatives with a full control on the E/Z selectivity. Several substrates bearing electron-donating and electron-withdrawing substituents were tolerable under the reaction conditions affording the corresponding products in good yields. This is the first study to report the synthesis of a vast array of novel 1,5-diphenylpent-3-en-1-yne derivatives paving the way for the preparation of tailored derivatives on mass scale necessary for biological studies and drug development.
Keywords :
PALLADIUM , B-Benzyl-9-BBN , B-Alkyl Suzuki coupling , Henna , Aqueous reaction