138540-75-7Relevant academic research and scientific papers
Efficient syntheses of the marine alkaloids makaluvamine D and discorhabdin C: The 4,6,7-trimethoxyindole approach
Sadanandan,Pillai,Lakshmikantham,Billimoria,Culpepper,Cava
, p. 1800 - 1805 (2007/10/02)
A new and efficient synthesis of the tricyclic quinonimine 20 as its trifluoroacetate 23 has been developed starting from the commercially available 2,4,5-trimethoxybenzaldehyde and proceeding via the hitherto unknown 4,6,7-trimethoxyindole (7). Quinonimi
Total synthesis of discorhabdin C: A general aza spiro dienone formation from O-silylated phenol derivatives using a hypervalent iodine reagent
Kita, Yasuyuki,Tohma, Hirofumi,Inagaki, Masanao,Hatanaka, Kenji,Yakura, Takayuki
, p. 2175 - 2180 (2007/10/02)
Hypervalent iodine oxidation of O-silylated phenols bearing various types of aminoquinones at the para position in 2,2,2-trifluoroethanol gave azacarbocyclic spiro dienones in good yields. Using this method, the first total synthesis of discorhabdin C, wh
