170421-35-9Relevant articles and documents
Synthetic studies of incednine: synthesis of C1-C13 pentaenoic acid segment
Ohtani, Takashi,Kanda, Hiroshi,Misawa, Kensuke,Urakawa, Yoshifumi,Toshima, Kazunobu
scheme or table, p. 2270 - 2273 (2009/08/07)
Stereoselective synthesis of the C1-C13 pentaenoic acid segment (4) of the novel antibiotic incednine (1) is described.
Efficient synthesis of the 6,6-spiroacetal of spirofungin A
Shimizu, Takeshi,Kusaka, Junichi,Ishiyama, Haruaki,Nakata, Tadashi
, p. 4965 - 4968 (2007/10/03)
The 6,6-spiroacetal segment of spirofungin A, an antifungal antibiotic isolated from Streptomyces violaceusniger Tü 4113, was efficiently prepared via the coupling reaction of the Weinreb amide and the alkyne which are readily available from the common in