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Results: 1-13 |
Results: 13
Synthesis of carba sugars from aldonolactones. Part IV. Stereospecific synthesis of carbaheptopyranoses by radical-induced carbocyclisation of 2,3-unsaturated octonolactones
Authors: Wagner, SH Lundt, I
Citation: Sh. Wagner et I. Lundt, Synthesis of carba sugars from aldonolactones. Part IV. Stereospecific synthesis of carbaheptopyranoses by radical-induced carbocyclisation of 2,3-unsaturated octonolactones, J CHEM S P1, (8), 2001, pp. 780-788
A study on the allylic substitution of (1R,5R,8R)- and (1R,5R,8S)-8-hydroxy-2-oxabicyclo[3.3.0]oct-6-en-3-one derivatives - Preparation of (1S,2R,3R)-9-[2-hydroxy-3-(2-hydroxyethyl)cyclopent-4-en-1-yl]-9H-adenine
Authors: Johansen, SK Lundt, I
Citation: Sk. Johansen et I. Lundt, A study on the allylic substitution of (1R,5R,8R)- and (1R,5R,8S)-8-hydroxy-2-oxabicyclo[3.3.0]oct-6-en-3-one derivatives - Preparation of (1S,2R,3R)-9-[2-hydroxy-3-(2-hydroxyethyl)cyclopent-4-en-1-yl]-9H-adenine, EUR J ORG C, (6), 2001, pp. 1129-1136
Synthetically useful base-induced rearrangements of aldonolactones
Authors: Lundt, I Madsen, R
Citation: I. Lundt et R. Madsen, Synthetically useful base-induced rearrangements of aldonolactones, T CURR CHEM, 215, 2001, pp. 177-191
Unusual ring contraction by substitution of 4-O-activated-pentono-1,5-lactams with cyanide. Stereospecific synthesis of 6-amino-1,4,5,6-tetradeoxy-1,4-imino-hexitols
Authors: Godskesen, M Lundt, I Sotofte, I
Citation: M. Godskesen et al., Unusual ring contraction by substitution of 4-O-activated-pentono-1,5-lactams with cyanide. Stereospecific synthesis of 6-amino-1,4,5,6-tetradeoxy-1,4-imino-hexitols, TETRAHEDR-A, 11(2), 2000, pp. 567-579
1,5-anhydro-D-fructose: Stereoselective conversions to 1,5-anhydroalditolsand deoxy/amino substituted analogues
Authors: Andersen, SM Lundt, I Marcussen, J
Citation: Sm. Andersen et al., 1,5-anhydro-D-fructose: Stereoselective conversions to 1,5-anhydroalditolsand deoxy/amino substituted analogues, J CARB CHEM, 19(6), 2000, pp. 717-725
A new stereospecific synthesis of 1,2,4-trideoxy-1,4-imino-D-erythro-pentitol
Authors: Malle, BM Lundt, I Furneaux, RH
Citation: Bm. Malle et al., A new stereospecific synthesis of 1,2,4-trideoxy-1,4-imino-D-erythro-pentitol, J CARB CHEM, 19(4-5), 2000, pp. 573-583
Syntheses of sugar-related trihydroxyazepanes from simple carbohydrates and their activities as reversible glycosidase inhibitors
Authors: Andersen, SM Ekhart, C Lundt, I Stutz, AE
Citation: Sm. Andersen et al., Syntheses of sugar-related trihydroxyazepanes from simple carbohydrates and their activities as reversible glycosidase inhibitors, CARBOHY RES, 326(1), 2000, pp. 22-33
Preparation of C-14-labelled 1,4-dideoxy-1,4-imino-D-arabinitol: Cyanosilylation of cyclic imines using KCN in a one-pot synthesis
Authors: Folkersen, BM Lundt, I Foged, C Valsborg, JS
Citation: Bm. Folkersen et al., Preparation of C-14-labelled 1,4-dideoxy-1,4-imino-D-arabinitol: Cyanosilylation of cyclic imines using KCN in a one-pot synthesis, J LABEL C R, 42(12), 1999, pp. 1145-1159
Synthesis of carbasugars from aldonolactones. Part II. Preparation of polyhydroxy/aminocyclopentanes functionalised at all five ring carbons
Authors: Johansen, SK Lundt, I
Citation: Sk. Johansen et I. Lundt, Synthesis of carbasugars from aldonolactones. Part II. Preparation of polyhydroxy/aminocyclopentanes functionalised at all five ring carbons, J CHEM S P1, (24), 1999, pp. 3615-3622
Highly functionalised cyclopentanes by radical cyclisation of unsaturated bromolactones III. Preparation of carbaaldohexofuranoses. Determination of the relative configuration at C-4/C-5 of 2,3-unsaturated heptono-1,4-lactones by means of H-1 NMR spectroscopy
Authors: Horneman, AM Lundt, I
Citation: Am. Horneman et I. Lundt, Highly functionalised cyclopentanes by radical cyclisation of unsaturated bromolactones III. Preparation of carbaaldohexofuranoses. Determination of the relative configuration at C-4/C-5 of 2,3-unsaturated heptono-1,4-lactones by means of H-1 NMR spectroscopy, SYNTHESIS-S, (2), 1999, pp. 317-325
Synthesis of carbasugars from aldonolactones: Ritter-type epoxide opening in the synthesis of polyhydroxylated aminocyclopentanes
Authors: Johansen, SK Korno, HT Lundt, I
Citation: Sk. Johansen et al., Synthesis of carbasugars from aldonolactones: Ritter-type epoxide opening in the synthesis of polyhydroxylated aminocyclopentanes, SYNTHESIS-S, (1), 1999, pp. 171-177
Deoxyiminoalditols from aldonic acids VI. Preparation of the four stereoisomeric 4-amino-3-hydroxypyrrolidines from bromodeoxytetronic acids. Discovery of a new alpha-mannosidase inhibitor
Authors: Limberg, G Lundt, I Zavilla, J
Citation: G. Limberg et al., Deoxyiminoalditols from aldonic acids VI. Preparation of the four stereoisomeric 4-amino-3-hydroxypyrrolidines from bromodeoxytetronic acids. Discovery of a new alpha-mannosidase inhibitor, SYNTHESIS-S, (1), 1999, pp. 178-183
1,5-anhydro-d-fructose: Regioselective acylation with fatty acids
Authors: Andersen, SM Lundt, I Marcussen, J Yu, SK
Citation: Sm. Andersen et al., 1,5-anhydro-d-fructose: Regioselective acylation with fatty acids, CARBOHY RES, 320(3-4), 1999, pp. 250-256
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