Year |
Citation |
Score |
2001 |
Stępowska H, Zamojski A. From methyl mannosides to methyl octosides by a stepwise homologation with Grignard C1 reagents Carbohydrate Research. 332: 429-438. PMID 11438099 DOI: 10.1016/S0008-6215(01)00103-3 |
0.374 |
|
2001 |
Grzeszczyk B, Zamojski A. Homologation of methyl 2-azido- and 2-acetamido-3,4-di-O-benzyl-2-deoxy-D-hexopyranosides with allyloxymethylmagnesium chloride. Carbohydrate Research. 332: 225-234. PMID 11434382 DOI: 10.1016/S0008-6215(01)00078-7 |
0.401 |
|
2000 |
Grzeszczyk B, Zamojski A. Homologation of O-Acetylated Methyl Hexopyranosides with a Grignard C1 Reagent Collection of Czechoslovak Chemical Communications. 65: 610-620. DOI: 10.1135/Cccc20000610 |
0.385 |
|
2000 |
Kim M, Grzeszczyk B, Zamojski A. Homologation of Protected Hexoses with Grignard C1 Reagents Tetrahedron. 56: 9319-9337. DOI: 10.1016/S0040-4020(00)00847-4 |
0.355 |
|
1999 |
Stępowska H, Zamojski A. Elongation of the pentose chain at the terminal carbon atom with Grignard C1 reagents. A study of the homologation reaction Tetrahedron. 55: 5519-5538. DOI: 10.1016/S0040-4020(99)00197-0 |
0.318 |
|
1999 |
Stępowska H, Zamojski A. The reaction of O-isopropylidene pentodialdo-1,4-furanoses with lithium diisopropylamide Carbohydrate Research. 321: 105-109. DOI: 10.1016/S0008-6215(99)00165-2 |
0.359 |
|
1999 |
Kim M, Grzeszczyk B, Zamojski A. From methyl d-glucopyranoside to methyl d-allopyranoside via the Mitsunobu reaction Carbohydrate Research. 320: 244-249. DOI: 10.1016/S0008-6215(99)00160-3 |
0.37 |
|
1998 |
Grzeszczyk B, Holst O, Müller-Loennies S, Zamojski A. Five monophosphates of methyl l-glycero-α-d-manno-heptopyranoside: synthesis, hydrolysis and migrations Carbohydrate Research. 307: 55-67. DOI: 10.1016/S0008-6215(98)00037-8 |
0.411 |
|
1997 |
Pakulski Z, Zamojski A. A route to 3-deoxy-4-O-methyl-D-manno-oct-2-ulosonic acid (4-O-methyl-KDO) and its D-gluco isomer derivatives Tetrahedron. 53: 3723-3728. DOI: 10.1016/S0040-4020(97)00094-X |
0.382 |
|
1997 |
Pakulski Z, Zamojski A. Diastereoselective propargylation of sugar aldehydes. New synthesis of 6-deoxyheptoses Tetrahedron. 53: 2653-2666. DOI: 10.1016/S0040-4020(96)01156-8 |
0.322 |
|
1997 |
Stêpowska H, Zamojski A. Synthesis of methyl d- and l-glycero-α-d-manno-heptofuranosides Carbohydrate Research. 304: 347-355. DOI: 10.1016/S0008-6215(97)00269-3 |
0.377 |
|
1996 |
Russa R, Urbanik-Sypniewska T, Shashkov AS, Banaszek A, Zamojski A, Mayer H. Partial Structure of Lipopolysaccharides Isolated from Rhizobium leguminosarum bv.trifolii 24 and Its GalA-Negative Exo− Mutant AR20 Systematic and Applied Microbiology. 19: 1-8. DOI: 10.1016/S0723-2020(96)80002-6 |
0.335 |
|
1996 |
Frelek J, Pakulski Z, Zamojski A. Application of [Mo2(OAc)4] for determination of absolute configuration of pyranoid and furanoid vic-diols by circular dichroism Tetrahedron-Asymmetry. 7: 1363-1372. DOI: 10.1016/0957-4166(96)00153-X |
0.305 |
|
1996 |
Grzeszczyk B, Holst O, Zamojski A. The synthesis of five l-glycero-d-manno-heptose monophosphates Carbohydrate Research. 290: 1-15. DOI: 10.1016/0008-6215(96)00105-X |
0.354 |
|
1995 |
Pakulski Z, Zamojski A. Separation of racemic binaphthol into enantiomers. Synthesis of neomenthylthioacetic acid chloride - a new chiral resolving agent Tetrahedron-Asymmetry. 6: 111-114. DOI: 10.1016/0957-4166(94)00365-I |
0.309 |
|
1995 |
Pakulski Z, Zamojski A. The reaction of acetyliron [(η5-C5H5)Fe(CO)(PPh3)(COCH3)] with sugar aldehydes. New synthesis of deoxysugars Tetrahedron. 51: 871-908. DOI: 10.1016/0040-4020(94)00978-4 |
0.425 |
|
1995 |
Banaszek A, Pakulski Z, Zamojski A. The synthesis of derivatives of 2,4-diamino-2,4,6-trideoxy-d-gulo- and l-altro-hexopyranoses Carbohydrate Research. 279: 173-182. DOI: 10.1016/0008-6215(95)00291-X |
0.376 |
|
1994 |
Nepogod'ev SA, Backinowski LV, Grzeszczyk B, Zamojski A. Synthesis of linear oligosaccharides: l-glycero-α-d-manno-heptopyranosyl derivatives of allyl α-glycosides of d-glucose, kojibiose, and 3-O-α-kojibiosyl-d-glucose, substrates for synthetic antigens Carbohydrate Research. 254: 43-60. PMID 8180996 DOI: 10.1016/0008-6215(94)84242-6 |
0.363 |
|
1994 |
Pakulski Z, Pierożyński D, Zamojski A. Reaction of sugar thiocyanates with Grignard reagents. New synthesis of thioglycosides. Tetrahedron. 50: 2975-2992. DOI: 10.1016/S0040-4020(01)87009-5 |
0.338 |
|
1994 |
Krajewski JW, Gluziński P, Pakulski Z, Zamojski A, Mishnev A, Kemme A. Synthesis, crystal structure, and conformation of methyl 6-deoxy-2,3-O-isopropylidene-α-d-manno-heptofuranoside Carbohydrate Research. 252: 97-105. DOI: 10.1016/0008-6215(94)90008-6 |
0.382 |
|
1994 |
Grzeszczyk B, Zamojski A. Benzyl 7-O-allyl-2,3-O-isopropylidene-4-O-p-methoxybenzyl-l-glycero-α-d-manno-heptopyranoside, a versatile ld-manHepp derivative☆ Carbohydrate Research. 262: 49-57. DOI: 10.1016/0008-6215(94)84004-0 |
0.36 |
|
1994 |
Stȩpowska H, Zamojski A. A Convenient Preparation of 5-Benzyl Ethers of D-Gluco- and D-Manno- furanose Derivatives. Carbohydrate Research. 265: 133-137. DOI: 10.1016/0008-6215(94)00216-9 |
0.312 |
|
1993 |
Guo ZW, Zamojski A, Krajewski JW, Gluziński P. Assignment of relative configurations and conformational analysis of α-phenylacyliron complexes (η5−C5H5)Fe(CO)(PPh3)(COCHRPh). X-ray structural determinations of two complexes (η5−C5H5)Fe(CO)(PPh3)(COCHPhR), R=CHOHCH3 and R=COH(CH3)2 Journal of Chemical Crystallography. 23: 209-221. DOI: 10.1007/Bf01190049 |
0.31 |
|
1992 |
Ramza J, Zamojski A. The synthesis of 5-C-(6-deoxy-1,2:3,4-di-O-isopropyidene- α-d-galactopyranos-6-yl)2,3-O-isopropylidene-d-allo- pentofuranose [deaminotri-O-isopropylidene tunicamine] Carbohydrate Research. 228: 205-216. PMID 1516087 DOI: 10.1016/S0008-6215(00)90560-3 |
0.358 |
|
1992 |
Nepogodev SA, Pakulski Z, Zamojski A, Holst O, Brade H. The synthesis and characterisation of 2-O-(6-O-l-glycero-α,β-d-manno-heptopyranosyl-α-d-glycopyranosyl)- α,β-d-glucopyranose☆ Carbohydrate Research. 232: 33-45. PMID 1423349 DOI: 10.1016/S0008-6215(00)90992-3 |
0.35 |
|
1992 |
Ramza J, Zamojski A. New convenient synthesis of tunicamine Tetrahedron. 48: 6123-6134. DOI: 10.1016/S0040-4020(01)89859-8 |
0.386 |
|
1991 |
Pakulski Z, Zamojski A, Holst O, Zähringer U. The synthesis and characterisation of 6-O-l-glycero-α-d-manno-heptopyranosyl-d-glucopyranose Carbohydrate Research. 215: 337-344. PMID 1794131 DOI: 10.1016/0008-6215(91)84032-A |
0.347 |
|
1990 |
Gawronski J, Radocki D, Jurczak J, Pakulski Z, Raczko J, Ramza J, Zamojski A. Exciton chirality method for establishing absolute configuration of 2-furylcarbinols The Journal of Organic Chemistry. 55: 1118-1120. DOI: 10.1021/Jo00290A061 |
0.569 |
|
1990 |
Krajewski JW, Gluziński P, Urbańczyk-Lipkowska Z, Ramza J, Zamojski A. X-ray and conformational investigation of 6-deoxy-7-C-(2-furyl)-1,2:3,4-di-O-isopropylidene-l-glycero-a-d-galacto- heptopyranose Carbohydrate Research. 200: 1-7. DOI: 10.1016/0008-6215(90)84178-W |
0.303 |
|
1990 |
Pakulski Z, Zamojski A. New observations on the Garegg-Samuelsson olefination reaction Carbohydrate Research. 205: 410-414. DOI: 10.1016/0008-6215(90)80160-5 |
0.334 |
|
1989 |
Karpiesiuk W, Banaszek A, Zamojski A. Nucleophilic displacement of the triflate group in benzyl 3-O-benzyl-4,6-O- benzylidene-2-O-trifluoromethanesulfonyl-α-d-mannopyranoside Carbohydrate Research. 186: 156-162. DOI: 10.1016/0008-6215(89)84013-3 |
0.304 |
|
1988 |
Grzeszczyk B, Banaszek A, Zamojski A. The synthesis of two repeating units of Haemophilus influenzae type a capsular antigen. Carbohydrate Research. 175: 215-226. PMID 3261200 DOI: 10.1016/0008-6215(88)84144-2 |
0.346 |
|
1988 |
Krajewski JW, Gluziński P, Urbańczyk-Lipkowska Z, Jarosz S, Zamojski A, Andreetti GD, Bocelli G. X-ray and conformational investigations of 7,8-dideoxy-1,2:3,4-di-O-isopropylidene-6-O-methyl-d-glycero-α-d-galacto-oct-7-ynopyranose ☆ Carbohydrate Research. 173: 151-157. DOI: 10.1016/S0008-6215(00)90810-3 |
0.338 |
|
1987 |
Dziewiszek K, Banaszek A, Zamojski A. The synthesis of the heptose region of the gram-negative bacterial core oligosaccharides Tetrahedron Letters. 28: 1569-1572. DOI: 10.1016/S0040-4039(01)81044-3 |
0.34 |
|
1987 |
Doboszewski B, Zamojski A. Convenient synthesis of a building-block derivative of nigerose Carbohydrate Research. 164: 470-476. DOI: 10.1016/0008-6215(87)80151-9 |
0.326 |
|
1986 |
Krajewski JW, Gluziński P, Urbańczyk-Lipkowska Z, Zamojski A, Andreetti GD, Bocelli G. Crystal and molecular structure of 1,2:3,4-Di-O-isopropylidene-6-O-toluene-p-sulfonyl-α-d-galactopyranose: Ring conformations in Di-O-isopropylidenegalactopyranose systems Carbohydrate Research. 148: 1-11. DOI: 10.1016/0008-6215(86)80031-3 |
0.33 |
|
1986 |
Dziewiszek K, Zamojski A. New syntheses of d- and l-glycero-d-manno-heptoses Carbohydrate Research. 150: 163-171. DOI: 10.1016/0008-6215(86)80013-1 |
0.384 |
|
1986 |
Grzeszczyk B, Dziewiszek K, Jarosz S, Zamojski A. Asymmetric Induction in Acid‐Catalysed Condensations of Sugar Aldehydes with Furan and 2‐Methylfuran. Cheminform. 17. DOI: 10.1002/Chin.198626306 |
0.335 |
|
1986 |
Krajewski JW, Gluzinski P, Jarosz S, Zamojski A, Bleidelis J, Mishnyov A, Kemme A. Synthesis, Crystal Structure and Conformation of 1(S)-Acetoxy-3-[6(R)- O-benzyl- 1,2 :3,4-di-O-isopropylidene-α-D-galactopyranos-6-yl]-1-(methyl-2,3,4-tri-O-benzyl- 6-deoxy-β-D-galactopyranosid-6-yl)propyne. Cheminform. 17. DOI: 10.1002/Chin.198623330 |
0.366 |
|
1985 |
Zamojski A, Grzeszczyk B, Banaszek A, Babiński J, Bordas X, Dziewiszek K, Jarosz S. Preparation and n.m.r.-spectral characteristics of benzyl-α,α-d2 ethers of monosaccharides Carbohydrate Research. 142: 165-171. DOI: 10.1016/S0008-6215(00)90747-X |
0.312 |
|
1985 |
Krajewski JW, Gluziński P, Jarosz S, Zamojski A, Bleidelis J, Mishnyov A, Ķemme A. Synthesis, crystal structure, and conformation of 1(S)-acetoxy-3-[6(R)-O-benzyl-1,2:3,4-di-O-isopropylidene-α-D-galactopyranos-6-yl]-1(methyl 2,3,4-tri-O-benzyl-6-deoxy-β-D-galactopyranosid-6-yl)propyne Carbohydrate Research. 144: 183-195. DOI: 10.1016/S0008-6215(00)90668-2 |
0.365 |
|
1985 |
Krajewski JW, Gluziński P, Urbańczyk-Lipkowska Z, Zamojski A, Luger P. Crystal and molecular structure of 6-C-(2-furyl)-1,2:3,4-di-O-isopropylidene-α-d-glycero-d-galacto-hexopyranose Carbohydrate Research. 139: 55-63. DOI: 10.1016/0008-6215(85)90006-0 |
0.326 |
|
1985 |
Chmielewski M, Doboszewski B, Achmatowicz OJ, Zamojski A. Synthesis of Lincomycin System. Part 3. Synthesis of Methyl 2,3,4,7-Tetra-O-acetyl-8-deoxy-α- und β-DL(LD)glycero-DL-galactooctopyranosid-6-ulose. Cheminform. 16. DOI: 10.1002/Chin.198527353 |
0.645 |
|
1985 |
Doboszewski B, Zamojski A. THE SYNTHESIS OF 2-O-α-D-GALACTOPYRANOSYL-D-GALACTOPYRANOSE AND 2-O-(2-O-α-D-GALACTOPYRANOSYL-α-D-GALACTOPYRANOSYL)-D-GLUCOPYRANOSE UNDECA-ACETATE Cheminform. 16. DOI: 10.1002/Chin.198507351 |
0.33 |
|
1984 |
Jaworska A, Zamojski A. A new method of oligosaccharide synthesis: Rhamnobioses Carbohydrate Research. 126: 191-203. DOI: 10.1016/0008-6215(84)85377-X |
0.348 |
|
1984 |
Doboszewski B, Zamojski A. The synthesis of 2-O-α-d-galactopyranosyl-d-galactopyranose and 2-O-(2-O-α-d-galactopyranosyl-α-d-galactopyranosyl)-d-glucopyranose undeca-acetate Carbohydrate Research. 132: 29-38. DOI: 10.1016/0008-6215(84)85061-2 |
0.343 |
|
1984 |
Chmielewski M, Achmatowicz OJ, Zamojski A. Stereoselective Synthesis of Methyl 3,4,7,8-Tetradeoxy-α-and β-DL-erythro-oct-3-enopyranosid-6-ulose Dimethyl Ketals. Cheminform. 15. DOI: 10.1002/Chin.198444327 |
0.63 |
|
1983 |
Koźluk T, Zamojski A. The synthesis of 3-deoxy-dl-streptose Tetrahedron. 39: 805-810. DOI: 10.1016/S0040-4020(01)91857-5 |
0.365 |
|
1983 |
Krajewski JW, Urbańczyk-Lipkowska Z, Gluziński P, Zamojski A, Stadnicka K. Crystal and molecular structures of benzyl 3-O-benzoyl-4-O-benzyl-2-O-(2,3,6-trideoxy-α-l-glycero-hex-2-enopyranosyl-4- ulose)-α-l-rhamnopyranoside Carbohydrate Research. 117: 13-22. DOI: 10.1016/0008-6215(83)88071-9 |
0.332 |
|
1983 |
Zamojski A, Banaszek A, Grynkiewicz G. The Synthesis Of Sugars From Non-Carbohydrate Substrates Cheminform. 14. DOI: 10.1002/Chin.198319348 |
0.306 |
|
1983 |
Dziewiszek K, Chmielewski M, Zamojski A. A New Synthesis Of D‐Glycero‐D‐Manno‐Heptose Cheminform. 14. DOI: 10.1002/Chin.198301340 |
0.314 |
|
1982 |
Zamojski A, Banaszek A, Grynkiewicz G. The Synthesis of Sugars from Non-Carbohydrate Substrates Advances in Carbohydrate Chemistry and Biochemistry. 40: 1-129. DOI: 10.1016/S0065-2318(08)60108-0 |
0.382 |
|
1982 |
Dziewiszek K, Chmielewski M, Zamojski A. A new synthesis of d-glycero-d-manno-heptose Carbohydrate Research. 104. DOI: 10.1016/S0008-6215(00)82228-4 |
0.3 |
|
1982 |
Jarosz S, Zamojski A. Asymmetric photocycloaddition between furan and optically active ketones Tetrahedron. 38: 1453-1456. DOI: 10.1016/0040-4020(82)80229-9 |
0.372 |
|
1982 |
Jarosz S, Zamojski A. Asymmetric photocycloaddition between furan and chiral alkyl glyoxylates Tetrahedron. 38: 1447-1451. DOI: 10.1016/0040-4020(82)80228-7 |
0.338 |
|
1982 |
Chmielewski M, Jurczak J, Zamojski A, Adamowicz H. The conformation of t-butyl 2-methoxy-5, 6-dihydro-2 H-pyran-6-carboxylates and 6,6′- disubstituted 2-methoxy-5,6-dihydro-2H-pyran derivatives on the basis of 1H and 13 C NMR spectra† Magnetic Resonance in Chemistry. 20: 249-253. DOI: 10.1002/Mrc.1270200412 |
0.607 |
|
1980 |
Grynkiewicz G, Zamojski A. Electrophilic Substitution of Aromatic Compounds by Unsaturated Sugar Derivatives Zeitschrift FüR Naturforschung B. 35: 1024-1027. DOI: 10.1515/Znb-1980-0818 |
0.317 |
|
1980 |
Chmielewski M, Banaszek A, Zamojski A, Adamowicz H. 13C-N.M.R. spectra of methyl 3,4-dideoxy-DL-glyc-3-enopyranosides Carbohydrate Research. 83: 3-7. DOI: 10.1016/S0008-6215(00)85358-6 |
0.322 |
|
1980 |
Priebe W, Zamojski A. The acid-catalysed reaction of thiols with alkyl 2,3-dideoxy-glyc-2-enopyranosides or glycals Tetrahedron. 36: 287-297. DOI: 10.1016/0040-4020(80)80017-2 |
0.313 |
|
1980 |
Grynkiewicz G, Zamojski A. Electrophilic Substitution Of Aromatic Compounds By Unsaturated Sugar Derivatives Cheminform. 11. DOI: 10.1002/Chin.198048298 |
0.317 |
|
1980 |
Grynkiewicz G, Krajewski JW, Urbanczyk-Lipkowska Z, Gluzinski P, Zamojski A. The O- Versus C-Alkylation During Reactions Of 6-Benzoyloxy-2H-Pyran-3(6H)-One With Phenols. Molecular Structure Of A New Benzofuran Derivative Cheminform. 11. DOI: 10.1002/Chin.198016194 |
0.336 |
|
1980 |
Jarosz S, Zamojski A. Rearrangement of 6-substituted 2,7-dioxabicyclo[3.2.0]hept-3-enes to furans Cheminform. 11. DOI: 10.1002/Chin.198007129 |
0.313 |
|
1979 |
Grynkiewicz G, Barszczak B, Zamojski A. Synthesis of 6-Alkoxy-2,3-dihydro-6H-pyran-3-ones from the 6-Acyloxy Derivatives Synthesis. 1979: 364-365. DOI: 10.1055/S-1979-28682 |
0.365 |
|
1979 |
Jarosz S, Zamojski A. Rearrangement of 6-substituted 2,7-dioxabicyclo[3.2.0]hept-3-enes to furans Journal of Organic Chemistry. 44: 3720-3723. DOI: 10.1021/Jo01335A024 |
0.354 |
|
1979 |
Chmielewski M, Konował A, Zamojski A. The synthesis of racemic purpurosamine B Carbohydrate Research. 70: 275-282. DOI: 10.1016/S0008-6215(00)87107-4 |
0.354 |
|
1979 |
Grynkiewicz G, Priebe W, Zamojski A. Synthesis of alkyl 4,6-di-o-acetyl-2,3-dideoxy-α-d-threo-hex-2- enopyranosides from 3,4,6-tri-o-acetyl-1,5-anhydro-2-deoxy- d-lyxo-hex-1-enitol (3,4,6-tri-o-acetyl-d-galactal) Carbohydrate Research. 68: 33-41. DOI: 10.1016/S0008-6215(00)84052-5 |
0.356 |
|
1979 |
BARANOWSKA E, PRIEBE W, ZAMOJSKI A, WALOCHA K. ChemInform Abstract: MASS SPECTROMETRY OF ALKYL 6-AMINO-4,6-DIDEOXY-1-THIO-α-DL-LYXO-HEXOPYRANOSIDES Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197929060 |
0.307 |
|
1978 |
Chmielewski M, Jurczak J, Zamojski A. The synthesis of 3,6-diamino-2,3,4,6-tetradeoxy-dl-threo-hexopyranose derivatives, substrates for the synthesis of negamycin Tetrahedron. 34: 2977-2981. DOI: 10.1016/0040-4020(78)88020-X |
0.652 |
|
1978 |
Chmielewski M, Mieczkowski J, Priebe W, Zamojski A, Adamowicz H. Configuration and conformation of methyl 2,3-anhydro-4-deoxy-pyranosides by 1H and 13C NMR spectra Tetrahedron. 34: 3325-3330. DOI: 10.1016/0040-4020(78)80251-8 |
0.353 |
|
1978 |
Grynkiewicz G, Zamojski A. The Synthesis Of 6‐Hydroxy‐2H‐Pyran‐3(6H)‐Onylhexoses, Potential Precursors Of Disaccharides Cheminform. 10: 491-496. DOI: 10.1002/Chin.197903312 |
0.369 |
|
1978 |
Jurczak J, Chmielewski M, Zamojski A. 2,4-Dideoxy-Dl-Hexoses: Basic Properties And Chemistry Cheminform. 9. DOI: 10.1002/Chin.197840320 |
0.546 |
|
1977 |
Zamojski A, Kozluk T. Synthesis of 3-substituted furans Journal of Organic Chemistry. 42: 1089-1090. DOI: 10.1021/Jo00426A038 |
0.376 |
|
1977 |
Mieczkowski J, Jurczak J, Chmielewski M, Zamojski A. The synthesis of 2,3-dideoxyhex-2-enono-1,5-lactones Carbohydrate Research. 56: 180-182. DOI: 10.1016/S0008-6215(00)84251-2 |
0.614 |
|
1977 |
Pyrek JS, Achmatowicz O, Zamojski A. Naphto- and anthraquinones of Streptomyces thermoviolaceusWR-141. Structures and model syntheses Tetrahedron. 33: 673-680. DOI: 10.1016/0040-4020(77)80309-8 |
0.601 |
|
1977 |
Pyrek JS, Achmatowicz OJ, Zamojski A. Naphtho- And Anthraquinones Of Streptomyces Thermoviolaceus Wr-141. Structure And Model Syntheses Cheminform. 8. DOI: 10.1002/Chin.197724372 |
0.576 |
|
1976 |
Konowal̵ A, Jurczak J, Zamojski A. Resolution and absolute configuration of trans (+)- and (−)-6-hydroxymethyl-2-methoxy-5,6-dihydro-2H-pyrans, substrates for total synthesis of monosaccharides Tetrahedron. 32: 2957-2959. DOI: 10.1016/0040-4020(76)80152-4 |
0.623 |
|
1976 |
Konowal A, Achmatowicz OJ, Zamojski A. Total Syntheses of Lincomycin System. Part 1. Synthesis of Three Methyl-6-acetamido-6,7,8-trideoxy-α-octopyranosides with (D-glycero-D-galacto, L-glycero-L-galacto),(D-glycero-D-allo, L-glycero-L-allo) and (D-glycero-D-altro, L-glycer Cheminform. 7. DOI: 10.1002/Chin.197642375 |
0.596 |
|
1976 |
Grynkiewicz G, Jurczak J, Zamojski A. REACTION OF 1,2-3,4-DI-O-ISOPROPYLIDENE-α-D-GALACTOPYRANOSE WITH DIALKYL AZODICARBOXYLATE IN THE PRESENCE OF TRIPHENYLPHOSPHINE Cheminform. 7. DOI: 10.1002/Chin.197629333 |
0.602 |
|
1976 |
Konowal A, Belniak K, Jurczak J, Chmielewski M, Achmatowicz OJ, Zamojski A. Derivatives Of 2-Alkoxy-5,6-Dihydro-2H-Pyran As Substrates In The Total Synthesis Of Monosaccharides. Part Xxi. The Synthesis Of 6-Acyl-2-Methoxy-5,6-Dihydro-2H-Pyrans Cheminform. 7. DOI: 10.1002/Chin.197629219 |
0.719 |
|
1976 |
Zamojski A, Burzynska H, Pietraszkiewicz M. The Synthesis Of Alkyl Glycosides From Monosaccharides And Dimethylformamide-Dialkyl Sulfate Adducts Cheminform. 7. DOI: 10.1002/Chin.197615383 |
0.401 |
|
1976 |
Achmatowicz OJ, Grynkiewicz G, Zamojski A. Conformation Of 4-(2-Furyl)-6-Methyl-5-Nitro-2-Phenyl- And 4-(2-Furyl)-2,2,6-Trimethyl-5-Nitro-1,3-Dioxanes Cheminform. 7. DOI: 10.1002/Chin.197602045 |
0.621 |
|
1975 |
Jurczak J, Grynkiewicz G, Zamojski A. The synthesis of N-glycosylphthalimides Carbohydrate Research. 39: 147-150. DOI: 10.1016/S0008-6215(00)82648-8 |
0.568 |
|
1975 |
Grynkiewicz G, Jurczak J, Zamojski A. The synthesis of mixed carbonates from alcohols, dialkyl azodicarboxylate and tris(dimethylamino)-phosphine Tetrahedron. 31: 1411-1414. DOI: 10.1016/0040-4020(75)87072-4 |
0.579 |
|
1975 |
Zwierzchowska-Nowakowska Z, Zamojski A. Allylic Rearrangement In 2-Acetoxy-5,6-Dihydro-2H-Pyran System Cheminform. 6. DOI: 10.1002/Chin.197510116 |
0.31 |
|
1974 |
Grynkiewicz G, Jurczak J, Zamojski A. New synthesis of monosaccharide carbonates Journal of the Chemical Society, Chemical Communications. 413-414. DOI: 10.1039/C39740000413 |
0.595 |
|
1974 |
Achmatowicz O, Banaszek A, Chmielewski M, Zamojski A, Lobodzinski W. Conformations of methyl 3,4-dideoxy-DL-glyc-3-enopyranosides Carbohydrate Research. 36: 13-22. DOI: 10.1016/S0008-6215(00)81988-6 |
0.623 |
|
1974 |
Grynkiewicz G, Jurczak J, Zamojski A. New Synthesis Of Monosaccharide Carbonates Cheminform. 5. DOI: 10.1002/Chin.197432445 |
0.577 |
|
1973 |
Chmielewski M, Zamojski A. Derivate Von 2-Alkoxy-5,6-Dihydro-Alpha-Pyran Als Substrate Bei Der Synth. Von Monosacchariden 18. Mitt. Synth. Von Acht Diastereomeren Methyl-Pentopyranosiden Cheminform. 4. DOI: 10.1002/Chin.197315487 |
0.33 |
|
1973 |
Chmielewski M, Zamojski A. Derivate Von 2-Alkoxy-5,6-Dihydro-Alpha-Pyran Als Substrate Bei Der Synth. Von Monosacchariden 16. Mitt. Synth. Von Methyl-3,4-Anhydro-Dl-Pentopyranosiden Cheminform. 4. DOI: 10.1002/Chin.197313481 |
0.335 |
|
1972 |
Jurczak J, Zamojski A. Condensation of 1-alkoxy-1,3-butadienes with optically active glyoxylic acid esters Tetrahedron. 28: 1505-1516. DOI: 10.1016/0040-4020(72)88033-5 |
0.595 |
|
1972 |
Achmatowicz O, Chmielewski M, Jurczak J, Kozerski L, Zamojski A. The NMR spectra and conformations of dihydropyran derivatives—II: The conformational energies of carbomethoxy, hydroxymethyl and acetoxymethyl groups at c‐6 of the 5,6‐dihydro‐α‐pyran ring Magnetic Resonance in Chemistry. 4: 537-545. DOI: 10.1002/Mrc.1270040413 |
0.718 |
|
1972 |
Achmatowicz OJ, Bukowski P, Grynkiewicz G, Szechner B, Zamojski A, Zwierzchowska Z. Cis-Trans-Isomere 2-Substituierter 2,5-Dimethoxy-2,5-Dihydro-Furane Cheminform. 3. DOI: 10.1002/Chin.197239080 |
0.57 |
|
1972 |
ACHMATOWICZ OJ, EJCHART A, JURCZAK J, KOZERSKI L, PYREK JS, ZAMOJSKI A. ChemInform Abstract: NMR-SPEKTREN UND KONFORM. VON DIHYDROPYRANDERIVATEN 3. MITT. ANWENDUNG VON TRIS-(DIPIVALOYLMETHANATO)-EUROPIUM(III) FUER 2-METHOXY-5,6-DIHYDRO-ALPHA-PYRAN- UND 2-METHOXY-TETRAHYDROPYRAN-DERIVATE Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197239075 |
0.716 |
|
1971 |
Achmatowicz O, Bukowski P, Szechner B, Zwierzchowska Z, Zamojski A. Synthesis of methyl 2,3-dideoxy-DL-alk-2-enopyranosides from furan compounds. A general approach to the total synthesis of monosaccharides Tetrahedron. 27: 1973-1996. DOI: 10.1016/S0040-4020(01)98229-8 |
0.65 |
|
1971 |
Banaszek A, Zamojski A. Derivate Des 2-Alkoxy-5,6-Dihydro-Alpha-Pyrans Als Substrate Fuer Die Synth. Von Monosacchariden 5. Mitt. Verlauf Der Ringoeffnung Des Oxiranringes Von Methyl-2,3-Anhydro-4,6-Didesoxy-Alpha-Dl-Lyxo- Und -Ribo-Hexopyranosiden Cheminform. 2. DOI: 10.1002/Chin.197131383 |
0.316 |
|
1971 |
Jurczak J, Zamojski A. Synth. Optisch Aktiver Glyoxylsaeureester Cheminform. 2. DOI: 10.1002/Chin.197114233 |
0.506 |
|
1971 |
Zamojski A, Konowal A, Jurczak J. Derivate Von 2-Alkoxy-5,6-Dihydro-Alpha-Pyran Als Substrate In Der Synthese Von Monosacchariden 1. Mitt. Stereochemie Der Addition Von Glyoxylsaeureestern An Trans-1-Methoxy-1,3-Butadien Cheminform. 2. DOI: 10.1002/Chin.197108201 |
0.601 |
|
1971 |
Konowal A, Zamojski A, Masojidkova M, Kohoutova J. Derivate Von 2-Alkoxy-5,6-Dihydro-Alpha-Pyran Als Substrate In Der Synthese Von Monosacchariden 4. Mitt. Stereochemie Der Epoxidation 6-Substituierter 2-Alkoxy-5,6-Dihydro-Alpha-Pyrane Cheminform. 2. DOI: 10.1002/Chin.197106313 |
0.304 |
|
1970 |
Zamojski A, Chmielewski M, Konował A. Four diastereoisomeric methyl esters of 2,4-dimethoxytetrahydropyran-6-carboxylic acid Tetrahedron. 26: 183-189. DOI: 10.1016/0040-4020(70)85018-9 |
0.359 |
|
1970 |
Achmatowicz O, Jurczak J, Konowal A, Zamojski A. The NMR spectra and conformations of dihydropyran derivatives—I: The conformations of 2‐alkoxy‐5,6‐dihydro‐α‐pyran‐6‐carboxylic esters Magnetic Resonance in Chemistry. 2: 55-62. DOI: 10.1002/Mrc.1270020107 |
0.698 |
|
1970 |
Jurczak J, Konowal A, Zamojski A. Derivate Des 2-Alkoxy-5,6-Dihydro-Alpha-Pyrans Als Substrate Bei Der Synthese Von Monosacchariden 3. Mitt. 2-Alkoxy-6-Hydroxymethyl-5,6-Dihydro-Alpha-Pyrane Und -Tetrahydropyrane Cheminform. 1. DOI: 10.1002/Chin.197050366 |
0.585 |
|
1970 |
Baranowska E, Jurczak J, Konowal A, Zamojski A. Massenspektren Von Di- Und Tetrahydropyranderivaten 4. Mitt. Fragmentierung Von 2-Alkoxy-6-Hydroxymethyl-5,6-Dihydro-Alpha-Pyranen (I) Und 2-Alkoxy-6-Hydroxymethyl-Tetrahydropyranen (Ii) Cheminform. 1. DOI: 10.1002/Chin.197023016 |
0.575 |
|
Low-probability matches (unlikely to be authored by this person) |
1976 |
Banaszek A, Zamojski A. The synthesis of racemic 4-deoxyneosamine C. Carbohydrate Research. 51: 276-279. PMID 1009539 DOI: 10.1016/S0008-6215(00)83337-6 |
0.3 |
|
1973 |
Chmielewski M, Zamojski A. Derivate Von 2-Alkoxy-5,6-Dihydro-Alpha-Pyran Als Substrate Bei Der Synth. Von Monosacchariden 11. Mitt. Synth. Und Eigenschaften Von Methyl-3,4-Didesoxy-Alpha- Und -Beta-Dl-Delta(3)-Pentenopyranosid Cheminform. 4. DOI: 10.1002/Chin.197309453 |
0.299 |
|
1970 |
Zamojski A, Chmielewski M, Konowal A. Derivate Von 2-Alkoxy-5,6-Dihydro-Alpha-Pyran Als Substrate Bei Der Synth. Von Monosacchariden 2. Mitt. Vier Diastereomere Methylester Von 2,4-Dimethoxy-Tetrahydropyran-6-Carbonsaeure Cheminform. 1. DOI: 10.1002/Chin.197017397 |
0.298 |
|
1998 |
Antonov KV, Backinowsky LV, Grzeszczyk B, Brade L, Holst O, Zamojski A. Synthesis and serological characterization of l-glycero-α-d-manno-heptopyranose-containing di- and tri-saccharides of the non-reducing terminus of the Escherichia coli K-12 LPS core oligosaccharide Carbohydrate Research. 314: 85-93. PMID 10230038 DOI: 10.1016/S0008-6215(98)00292-4 |
0.297 |
|
1990 |
Holst O, Brade H, Dziewiszek K, Zamojski A. G.l.c.-m.s. of partially methylated and acetylated derivatives of l-glycero-d-manno- and d-glycero-d-manno-heptopyranoses and -heptitols Carbohydrate Research. 204: 1-9. PMID 2279240 DOI: 10.1016/0008-6215(90)84016-N |
0.296 |
|
1974 |
Zwierzchowska-Nowakoska Z, Zamojski A. Products Of Reactions Of D-Glucal And 3,4,6-Tri-O-Acetyl-D-Glucal With Methanol In The Presence Of Hydrogen Chloride Cheminform. 5. DOI: 10.1002/Chin.197441423 |
0.295 |
|
1991 |
Holst O, Zähringer U, Brade H, Zamojski A. Structural analysis of the heptose/hexose region of the lipopolysaccharide from Escherichia coli K-12 strain W3100. Carbohydrate Research. 215: 323-335. PMID 1794130 DOI: 10.1016/0008-6215(91)84031-9 |
0.292 |
|
1996 |
Wiśniewski K, Pakulski Z, Zamojski A, Sheldrick WS. Synthesis, alkylation, crystal structure and molecular mechanics investigations of the (methylthio) acetyliron complex [(η5-C5H5)Fe(CO)(PPh3)COCH2SCH3] Journal of Organometallic Chemistry. 523: 1-7. DOI: 10.1016/0022-328X(96)06340-1 |
0.29 |
|
1985 |
Grzeszczyk B, Dziewiszek K, Jarosz S, Zamojski A. Asymmetric induction in acid-catalysed condensations of sugar aldehydes with furan and 2-methylfuran☆ Carbohydrate Research. 145: 145-151. DOI: 10.1016/S0008-6215(00)90422-1 |
0.288 |
|
1971 |
Achmatowicz OJ, Bukowski P, Szechner B, Zwierzchowska Z, Zamojski A. Synth. Von Methyl-2,3-Didesoxy-Dl-Alk-2-Enopyranosiden Aus Furan-Verbindungen, Allgemeine Methode Fuer Die Totalsynth. Von Monosacchariden Cheminform. 2. DOI: 10.1002/Chin.197137371 |
0.288 |
|
1986 |
Banaszek A, Cornet XB, Zamojski A. A New, Efficient Method for Hydrolysis of the Anomeric Acetyl Group in Substituted Hexopyranoses. Cheminform. 17. DOI: 10.1002/Chin.198623326 |
0.287 |
|
1985 |
Banaszek A, Cornet XB, Zamojski A. A new, efficient method for hydrolysis of the anomeric acetyl group in substituted hexopyranoses Carbohydrate Research. 144: 342-345. DOI: 10.1016/S0008-6215(00)90683-9 |
0.287 |
|
1975 |
Zwierzchowska-Nowakowska Z, Zamojski A. Reaction Of 4-Acetoxy-2,3-Dihydro-4H-Pyrans And 2-Acetoxy-5,6-Dihydro-2H-Pyrans With Methanol In Presence Of Hydrogen Chloride Cheminform. 6. DOI: 10.1002/Chin.197512267 |
0.277 |
|
1973 |
Krowicki K, Zamojski A. Chemical Modification Of Erythromycins The Journal of Antibiotics. 26: 569-574. PMID 4792102 DOI: 10.7164/Antibiotics.26.569 |
0.274 |
|
1996 |
Guo ZW, Zamojski A. Elaboration of the acyl ligand in complex (η5-C5H5)Fe(CO)(PPh3)(COCH2Ph) Tetrahedron. 52: 12553-12570. DOI: 10.1016/0040-4020(96)00745-4 |
0.274 |
|
1972 |
Chmielewski M, Zamojski A. 2-Alkoxy-5,6-Dihydro-Alpha-Pyranderivate Als Substrate Bei Der Synth. Von Monosacchariden 7. Mitt. Stereochemie Der Bromaddition An 6-Substituierte 2-Methoxy-5,6-Dihydro-Alpha-Pyrane Cheminform. 3. DOI: 10.1002/Chin.197205117 |
0.271 |
|
1993 |
Frelek J, Pakulski Z, Zamojski A. Circular Dichroism of Transition Metal Complexes and Sugar Derivatives Having a Free 1,3-Diol System or “Isolated” Hydroxyl Group Journal of Carbohydrate Chemistry. 12: 625-639. DOI: 10.1080/07328309308019412 |
0.268 |
|
2002 |
Kim M, Grzeszczyk B, Zamojski A. Improving the stereoselectivity of one-carbon atom homologation of hexoses at the terminal position Tetrahedron Letters. 43: 1337-1340. DOI: 10.1016/S0040-4039(01)02376-0 |
0.267 |
|
1998 |
Wiśniewski K, Zamojski A, Rogers RD. (Phenylthio)acetyliron complex [(η5-C5H5)Fe(CO)(PPh3)COCH2SPh] configuration of aldols Tetrahedron. 54: 14201-14212. DOI: 10.1016/S0040-4020(98)00874-6 |
0.261 |
|
1972 |
Chmielewski M, Jurezak J, Zamojski A. Derivate Des 2‐Alkoxy‐5,6‐Dihydro‐Alpha‐Pyrans Als Substrate Bei Der Synth. Von Monosacchariden 10. Mitt. Stereochemie Der Addition Von Essigsaeure Mit 6‐Acetoxymethyl‐2‐Methoxy‐5,6‐Dihydro‐Alpha‐Pyran Cheminform. 3. DOI: 10.1002/Chin.197236441 |
0.258 |
|
1992 |
Guo ZW, Zamojski A. Base-dependent stereoselectivity in reactions of acyl ligand in phenylacetyliron complex (η5-C5H5)Fe(CO)(PPh3)(COCH2Ph) Tetrahedron Letters. 33: 1105-1108. DOI: 10.1016/S0040-4039(00)91872-0 |
0.252 |
|
1971 |
Konowal A, Zamojski A. Derivate Von 2‐Alkoxy‐5,6‐Dihydro‐Alpha‐Pyran Als Substrate In Der Synth. Von Monosacchariden 6. Mitt. Synth. Von Vier Diastereomeren Methyl‐4‐Desoxy‐Dl‐Hexopyranosiden Cheminform. 2. DOI: 10.1002/Chin.197139363 |
0.248 |
|
1976 |
Banaszek A, Szechner B, Mieczkowski J, Zamojski A. The Reaction Of Unsaturated Monosaccharides With Triphenyl Phosphine, Phthalimide And Diethyl Azodicarboxylate Cheminform. 7. DOI: 10.1002/Chin.197621330 |
0.247 |
|
1999 |
Bartnicka E, Zamojski A. New Syntheses Of Two Epimers Of (+)-Castanospermine : (+)-8A-Epi- And (+)-1,8A-Di-Epi-Castanospermine Tetrahedron. 55: 2061-2076. DOI: 10.1016/S0040-4020(98)01218-6 |
0.243 |
|
1993 |
Stȩpowska H, Zamojski A. Alkylation and aldol reactions of acyl and phosphine ligand in (η5-C5H5)Fe(CO)(CH3PPh2)(COCH2R) Journal of Organometallic Chemistry. 456: 221-228. DOI: 10.1016/0022-328X(93)80429-F |
0.242 |
|
1972 |
Banaszek A, Zamojski A. Derivate Von 2‐Alkoxy‐5,6‐Dihydro‐Alpha‐Pyran Als Substrate Bei Der Synth. Von Monosacchariden 8. Mitt. Synth. Von ′Beta‐Lyxo′‐Epoxiden Aus 6‐Substituierten 2‐Alkoxy‐5,6‐Dihydro‐Alpha‐Pyranen Cheminform. 3. DOI: 10.1002/Chin.197213483 |
0.241 |
|
1979 |
Jankowski K, Bélanger J, Söler F, Zamojski A. Equation de Karplus appliquée à des systèmes sp2–sp3 Magnetic Resonance in Chemistry. 12: 544-547. DOI: 10.1002/Mrc.1270120908 |
0.24 |
|
1991 |
Krajewski JW, Gluziński P, Zamojski A, Mishnyov A, Kemme A, Zhong-Wu G. X-ray structural and molecular mechanics investigations of cyclopentadienyl-carbonyl-triphenylphosphine-methoxyacetyl-iron (η5-C5H5)Fe(CO)(PPh3)(COCH2OMe) Journal of Chemical Crystallography. 21: 271-275. DOI: 10.1007/Bf01156077 |
0.237 |
|
2001 |
Shashkov AS, Pakulski Z, Grzeszczyk B, Zamojski A. Distribution of pyranose and furanose forms of 6-deoxyheptoses in water solution. Carbohydrate Research. 330: 289-294. PMID 11270807 DOI: 10.1016/S0008-6215(00)00309-8 |
0.231 |
|
1997 |
Akritopoulou-Zanze I, Nakanishi K, Stepowska H, Grzeszczyk B, Zamojski A, Berova N. Configuration of heptopyranoside and heptofuranoside side chains: 2‐anthroate, a powerful chromophore for exciton coupled CD Chirality. 9: 699-712. PMID 9366030 DOI: 10.1002/(Sici)1520-636X(1997)9:7<699::Aid-Chir11>3.0.Co;2-I |
0.229 |
|
1973 |
Krowicki K, Zamojski A. Chemical modification of erythromycins. II. 8-hydroxyerythromycin A. The Journal of Antibiotics. 26: 575-581. PMID 4792103 DOI: 10.7164/Antibiotics.26.575 |
0.224 |
|
1987 |
Jarosz S, Głodek J, Zamojski A. Inversion of configuration at the propargylic alcohol center in sugar acetylenes Carbohydrate Research. 163: 289-296. DOI: 10.1016/0008-6215(87)80192-1 |
0.218 |
|
1973 |
Krowicki K, Zamojski A. Chemical modification of erythromycins. 3. Spiroketals of 8-hydroxyerythromycin A. The Journal of Antibiotics. 26: 582-586. PMID 4792104 DOI: 10.7164/Antibiotics.26.582 |
0.212 |
|
1995 |
Baranowska E, Danikiewicz W, Pakulski Z, Zamojski A. Fragmentation of (η5-cyclopentadienyl)dicarbonyl-acyliron complexes under electron impact Journal of Mass Spectrometry. 30: 158-162. DOI: 10.1002/Jms.1190300124 |
0.196 |
|
1970 |
Konowal A, Zamojski A. Chemische Verschiebung Der Glykosidischen Methylgruppe In Pyranosiden Cheminform. 1. DOI: 10.1002/Chin.197050158 |
0.191 |
|
1968 |
Banaszek A, Krowicki K, Zamojski A. Thin-layer and column chromatography of erythoromycins andsome degradation products Journal of Chromatography A. 32: 581-583. PMID 4295864 DOI: 10.1016/S0021-9673(01)80531-8 |
0.19 |
|
1970 |
Zwierzchowska Z, Zamojski A. Modell Der ′Glykal-Pseudoglykal′-Umlagerung Cheminform. 1. DOI: 10.1002/Chin.197050248 |
0.189 |
|
Hide low-probability matches. |