691006-75-4Relevant academic research and scientific papers
Total synthesis of (+)-batzelladine A and (-)-batzelladine D, and identification of their target protein
Shimokawa, Jun,Ishiwata, Takanori,Shirai, Koji,Koshino, Hiroyuki,Tanatani, Aya,Nakata, Tadashi,Hashimoto, Yuichi,Nagasawa, Kazuo
, p. 6878 - 6888 (2007/10/03)
Asymmetric total synthesis of batzelladine A (1) and batzelladine D (2) has been achieved. Our synthesis of batzelladines features 1) stereoselective construction of the cyclic guanidine system by means of successive 1,3-dipolar cycloaddition reaction and
Enantioselective total synthesis of batzelladine A
Shimokawa, Jun,Shirai, Koji,Tanatani, Aya,Hashimoto, Yuichi,Nagasawa, Kazuo
, p. 1559 - 1562 (2007/10/03)
One-step formation of an enone from a primary alcohol has been effectively applied in the total synthesis of batzelladine A (1). Successive 1,3-dipolar cycloadditions with a subsequent cyclization were used to form the tricyclic guanidine subunit of this
