643016-60-8Relevant articles and documents
Stereocontrolled Total Synthesis of Nonenolide
Sudina, Purushotham Reddy,Motati, Damoder Reddy,Seema, Aravind
, p. 1399 - 1404 (2018/06/29)
Nonenolide (1) was first isolated from the entomopathogenic fungus Cordyceps militaries BCC2816 and exhibited good antimalarial activity against Plasmodium falciparum K1. Structurally, it features a decanolide with a trans-double bond attached to two chir
Asymmetric total synthesis of paecilomycin E, 10′-epi-paecilomycin e and 6′-epi-cochliomycin C
Pal, Pratik,Jana, Nandan,Nanda, Samik
supporting information, p. 8257 - 8274 (2015/01/08)
The asymmetric total syntheses of naturally occurring resorcylic acid lactone paecilomycin E and two of its structural congeners have been reported in this article. The major highlight of the synthetic venture is the application of the late stage Mitsunob
Synthetic studies on macrolactin A by using a (diene)Fe(CO)3 complex
Fukuda, Akihiro,Kobayashi, Yusuke,Kimachi, Tetsutaro,Takemoto, Yoshiji
, p. 9305 - 9313 (2007/10/03)
The stereoselective synthesis of the two segments 3 and 4 of macrolactin A 1 is described. Macrolactin A is a 24-membered polyene macrolide antibiotic, which is of interest due to a strong activity against B16-F10 murine tumor cell and HIV-1 virus. The ke