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Results: 1-8 |
Results: 8
Fluorescent-labeled derivatives of dolichyl phosphate. Analogs of dolichylphosphate with the 2-aminopyridine residue at the omega-end of the chain
Authors: Veselovsky, VV Lozanova, AV Maltsev, SD Danilov, LL Shibaev, VN Jedrzejas, MJ
Citation: Vv. Veselovsky et al., Fluorescent-labeled derivatives of dolichyl phosphate. Analogs of dolichylphosphate with the 2-aminopyridine residue at the omega-end of the chain, RUSS CHEM B, 50(3), 2001, pp. 531-536
A new version of the conversion of plant polyprenols into (+/-)-terpenols of the dolichol series
Authors: Veselovsky, VV Lozanova, AV
Citation: Vv. Veselovsky et Av. Lozanova, A new version of the conversion of plant polyprenols into (+/-)-terpenols of the dolichol series, RUSS CHEM B, 49(8), 2000, pp. 1485-1486
A novel polyfunctional chiral building block derived from (S)-ethyl lactate. Application to the synthesis of the sex pheromone of the southern corn rootworm (Diabrotica undecimpunctata howardi)
Authors: Zlokazov, MV Veselovsky, VV
Citation: Mv. Zlokazov et Vv. Veselovsky, A novel polyfunctional chiral building block derived from (S)-ethyl lactate. Application to the synthesis of the sex pheromone of the southern corn rootworm (Diabrotica undecimpunctata howardi), RUSS CHEM B, 49(1), 2000, pp. 154-158
Synthesis of dolichyl phosphate derivatives with fluorescent label at the omega-end of the chain, new tools to study protein glycosylation
Authors: Shibaev, VN Veselovsky, VV Lozanova, AV Maltsev, SD Danilov, LL Forsee, WT Xing, J Cheung, HC Jedrzejas, MJ
Citation: Vn. Shibaev et al., Synthesis of dolichyl phosphate derivatives with fluorescent label at the omega-end of the chain, new tools to study protein glycosylation, BIOORG MED, 10(2), 2000, pp. 189-192
Chemo- and regioselective nitration of geranylacetone by NaNO2/AcOH. Synthesis of 6,10-dimethyl-9-methyleneundec-5E-en-2-one
Authors: Stepanov, AV Veselovsky, VV
Citation: Av. Stepanov et Vv. Veselovsky, Chemo- and regioselective nitration of geranylacetone by NaNO2/AcOH. Synthesis of 6,10-dimethyl-9-methyleneundec-5E-en-2-one, RUSS CHEM B, 48(7), 1999, pp. 1287-1290
A simple method for preparing racemic dolichols from the polyprenols of pine needles (Pinus silvestris)
Authors: Veselovsky, VV
Citation: Vv. Veselovsky, A simple method for preparing racemic dolichols from the polyprenols of pine needles (Pinus silvestris), RUSS CHEM B, 48(5), 1999, pp. 1000-1002
A new approach to the synthesis of a polyfunctional acyclic chiral building block based on ethyl (S)-(-)-lactate
Authors: Zlokazov, MV Veselovsky, VV
Citation: Mv. Zlokazov et Vv. Veselovsky, A new approach to the synthesis of a polyfunctional acyclic chiral building block based on ethyl (S)-(-)-lactate, MENDELEEV C, (2), 1999, pp. 73-74
Chemistry of natural compounds and bioorganic chemistry - Stereocontrolledsynthesis of the alkaloid (-)-actinidine
Authors: Stepanov, AV Lozanova, AV Veselovsky, VV
Citation: Av. Stepanov et al., Chemistry of natural compounds and bioorganic chemistry - Stereocontrolledsynthesis of the alkaloid (-)-actinidine, RUSS CHEM B, 47(11), 1998, pp. 2286-2291
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