158818-92-9Relevant academic research and scientific papers
Total Synthesis and Absolute Configuration of Simpotentin, a Potentiator of Amphotericin B Activity
Ohtawa, Masaki,Shimizu, Eri,Saito, Atsushi,Sakamoto, Sayuri,Waki, Ai,Kondo, Ariko,Yagi, Akiho,Uchida, Ryuji,Tomoda, Hiroshi,Nagamitsu, Tohru
, p. 5596 - 5599 (2019)
The total synthesis of simpotentin (1), a new potentiator of amphotericin B activity against Candida albicans, was achieved. Our research results enabled the access of all stereoisomers of 1 and the elucidation of the unknown absolute configuration of 1.
3,4,6-Tri-O-benzyl-α-D-arabino-hexopyranos-2-ulosyl Bromide: A Versatile Glycosyl Donor for the Efficient Generation of β-D-Mannopyranosidic Linkages
Lichtenthaler, Frieder W.,Schneider-Adams, Thomas
, p. 6728 - 6734 (2007/10/02)
An expedient four-step sequence is described for the conversion of acetobromoglucose into the title 2-oxohexosyl ("ulosyl") bromide 4.Due to its O-benzyl protection, 4 is considerably more reactive than its acylated analogs 1-3: Ag2CO3-promoted glycosidat
