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Results: 1-8 |
Results: 8
NMR structure determination of brefeldin-A, a 13-membered ring fungal metabolite
Authors: Glaser, R Shiftan, D Froimowitz, M
Citation: R. Glaser et al., NMR structure determination of brefeldin-A, a 13-membered ring fungal metabolite, MAGN RES CH, 38(4), 2000, pp. 274-280
Mobility of lipid in complexes of amylose-fatty acids by deuterium and C-13 solid state NMR
Authors: Lebail, P Buleon, A Shiftan, D Marchessault, RH
Citation: P. Lebail et al., Mobility of lipid in complexes of amylose-fatty acids by deuterium and C-13 solid state NMR, CARBOHY POL, 43(4), 2000, pp. 317-326
Change in the V/B polymorph ratio and T-1 relaxation of epichlorohydrin crosslinked high amylose starch excipient
Authors: Shiftan, D Ravenelle, F Mateescu, MA Marchessault, RH
Citation: D. Shiftan et al., Change in the V/B polymorph ratio and T-1 relaxation of epichlorohydrin crosslinked high amylose starch excipient, STARCH, 52(6-7), 2000, pp. 186-195
Conformational pseudopolymorphism and solid-state CPMAS NMR studies for determination of solvent-dependent solution-state conformational preferences for (-)-scopolamine hydrobromide/hydrochloride salts (vol 64, pg 9219, 1999)
Authors: Glaser, R Shiftan, D Drouin, M
Citation: R. Glaser et al., Conformational pseudopolymorphism and solid-state CPMAS NMR studies for determination of solvent-dependent solution-state conformational preferences for (-)-scopolamine hydrobromide/hydrochloride salts (vol 64, pg 9219, 1999), J ORG CHEM, 65(6), 2000, pp. 1898-1898
Eight-membered-ring solid-state conformational interconversion via the atom-flip mechanism, a CPMAS C-13 NMR and crystallographic stereochemical study
Authors: Glaser, R Novoselsky, A Shiftan, D Drouin, M
Citation: R. Glaser et al., Eight-membered-ring solid-state conformational interconversion via the atom-flip mechanism, a CPMAS C-13 NMR and crystallographic stereochemical study, J ORG CHEM, 65(20), 2000, pp. 6345-6353
The solid-state structures of (-)-scopolamine free base, (-)-scopolamine methobromide, (-)-scopolamine hydrobromide trihydrate, and of the pseudopolymorphic forms of (-)-scopolamine hydrochloride anhydrate and 1.66hydrate
Authors: Glaser, R Shiftan, D Drouin, M
Citation: R. Glaser et al., The solid-state structures of (-)-scopolamine free base, (-)-scopolamine methobromide, (-)-scopolamine hydrobromide trihydrate, and of the pseudopolymorphic forms of (-)-scopolamine hydrochloride anhydrate and 1.66hydrate, CAN J CHEM, 78(2), 2000, pp. 212-223
Conformational pseudopolymorphism and solid-state CPMAS NMR studies for determination of solvent-dependent solution-state conformational preferences for (-)-scopolamine hydrobromide/hydrochloride salts
Authors: Glaser, R Shiftan, D Drouin, M
Citation: R. Glaser et al., Conformational pseudopolymorphism and solid-state CPMAS NMR studies for determination of solvent-dependent solution-state conformational preferences for (-)-scopolamine hydrobromide/hydrochloride salts, J ORG CHEM, 64(25), 1999, pp. 9217-9224
The stereochemistry and interconversion of nine-membered rings containing one strong torsional constraint
Authors: Glaser, R Shiftan, D
Citation: R. Glaser et D. Shiftan, The stereochemistry and interconversion of nine-membered rings containing one strong torsional constraint, ADV MOL STR, 5, 1999, pp. 89-151
Risultati: 1-8 |