151075-88-6Relevant academic research and scientific papers
Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potent α-glucosidase inhibitors
Xie, Weijia,Tanabe, Genzoh,Akaki, Junji,Morikawa, Toshio,Ninomiya, Kiyofumi,Minematsu, Toshie,Yoshikawa, Masayuki,Wu, Xiaoming,Muraoka, Osamu
experimental part, p. 2015 - 2022 (2011/05/05)
Two hitherto missing members of sulfonium salts family in Salacia genus plants as a new class of α-glucosidase inhibitors, neoponkoranol (7) and neosalaprinol (8), were isolated from the water extracts, and their structures were unambiguously identified.
α-Fluorinated phosphonates as substrate mimics for glucose 6-phosphate dehydrogenase: The CHF stereochemistry matters
Berkowitz, David B.,Bose, Mohua,Pfannenstiel, Travis J.,Doukov, Tzanko
, p. 4498 - 4508 (2007/10/03)
Reported is a systematic study of the 'fitness' (in terms of k(cat)/K(m)) of a series of phosphonate mimics of glucose 6-phosphate (G6P) as unnatural substrates for G6P dehydrogenase from Leuconostoc mesenteroides. The four G6P analogues (9, 10, 15a, and 15b) differ only in the degree of fluorination at the 'bridging' phosphonate carbon. All have been synthesized from benzyl 6-O-trifluoromethane-sulfonyl-2,3,4-tri-O-benzyl β-D-glucopyranoside (6). The phosphonates with bridging CH2 (9) and CF2 (10) groups are cleanly obtained by direct displacements with the appropriate LiX2CP(O)(OEt)2 reagents (X = H, F) in 15 min at -78 °C. For the (α-monofluoro)alkylphosphonates (15a/b), homologation of 6 is achieved via lithiodithiane-mediated triflate displacement, followed by aldehyde unmasking [CaCO3, Hg(ClO4)2, H2O]. Addition of diethyl phosphite anion produces diastereomeric, (α-hydroxy)phosphonates 13a/b (1.4:1 ratio) which may be readily separated by chromatography. The stereochemistry of the minor diastereomer was established as 7(S) via X-ray crystallographic structure determination of its p-bromobenzoate derivative, 16b. Treatment of the major 7(R) diastereomer with DAST produces α-fluorinated phosphonate 14a, in modest yield, with inversion of configuration, as established, again, by X-ray crystallography. To our knowledge, this is first example of DAST-mediated fluorination of a (nonbenzylic, nonpropargylic) secondary (α-hydroxy)-phosphonate and thus establishes the stereochemical course of this transformation. α-Deprotonation/kinetic quenching of 14a provides access to the 7(R)-epimer (14b). For all four protected phosphonates (7, 8, 14a, and 14b), diethyl phosphonate ester deprotection was carried out with TMSBr, followed by global hydrogenolytic debenzylation to produce the free phosphonates, as α/β anomeric mixtures. Titrations of G6P itself and the free phosphonic acids provides second pK(a) values of 6.5 (1, bridging-O), 5.4 (10, bridging-CF2), 6.2 (14a, bridging-CHF), and 7.6 (9, bridging-CH2). Leuconostoc mesenteroides G6PDH-mediated oxidation and Lineweaver-Burk analysis yields normalized k(cat)/K(m) values of 0.043 (14b, bridging-7(R)-CHF), 0.11 (10, bridging-CF2), 0.23 (14b, bridging-CH2), and 0.46 (14a, bridging-7(S)-CHF) relative to G6P itself, largely reflecting differences in K(m). The fact that k(cat)/K(m) increases by more than an order of magnitude in going from the 7(R)-α-monofluoroalkyl phosphonate (worst substrate) to the 7(S)-diastereomer (best substrate) is especially notable and is discussed in the context of the known phosphate binding pocket of this enzyme as revealed by X-ray crystallography (Adams, M. J. et al. Structure 1994, 2, 1073-1087).
Synthesis of (α,α-Difluoroalkyl)phosphonates by Displacement of Primary Triflates
Berkowitz, David B.,Eggen, MariJean,Shen, Quanrong,Sloss, Darby G.
, p. 6174 - 6176 (2007/10/02)
Simple primary alkyl triflates and those derived from several monosaccharides are cleanly displaced by diethyl(lithiodifluoromethyl)phosphonate to provide the corresponding (α,α-difluoroalkyl)phosphonates in minutes at -78 deg C.
