83866-10-8Relevant articles and documents
Total synthesis of kehokorins A and B
Fujiwara, Kenshu,Motousu, Ryosuke,Sato, Daisuke,Kondo, Yoshihiko,Akiba, Uichi,Suzuki, Takanori,Tokiwano, Tetsuo
, p. 1299 - 1301 (2019)
The total synthesis of a dibenzofuran rhamnoside, kehokorin A, and its aglycone, kehokorin B, was achieved via a route including Suzuki-Miyaura cross-coupling followed by Ullmann ether synthesis to form a dibenzofuran, stepwise bromination at C7 of the di
Synthesis of Rhamnolipid Derivatives Containing Ester Isosteres
Lowary, Todd L.,Wang, Lei
supporting information, p. 9633 - 9637 (2020/12/21)
Rhamnolipids are biosurfactants with many applications, arising from their inherent biological activity and their potential as bioremediation agents. Herein, we report the synthesis of four rhamnolipid derivatives in which the ester linkage connecting the
Synthesis of the rhamnosyl trisaccharide repeating unit to mimic the antigen determinant of Pseudomonas syringae lipopolysaccharide
Yu, Chung-Shan,Wang, Heng-Yen,Chiang, Li-Wu,Pei, Kai
, p. 1412 - 1420 (2008/02/13)
The trisaccharide 2,3,4-O-tribenzyl-α-L-rhamnosyl-(1→3)-4-O- acetyl-2-O-benzoyl-(1→2)-4-O-acetyl-3-O-benzoyl-α-L-rhamnosyl-1-(4- tolyl)thio-α-L-rhamnopyranoside was prepared from the thio-sugar 1-(4-tolyl)thio-α,β-L-rhamnopyranoside from the nonreducing e