PL111474B1 - Process for preparing novel neamine drivatives - Google Patents
Process for preparing novel neamine drivatives Download PDFInfo
- Publication number
- PL111474B1 PL111474B1 PL1976192253A PL19225376A PL111474B1 PL 111474 B1 PL111474 B1 PL 111474B1 PL 1976192253 A PL1976192253 A PL 1976192253A PL 19225376 A PL19225376 A PL 19225376A PL 111474 B1 PL111474 B1 PL 111474B1
- Authority
- PL
- Poland
- Prior art keywords
- formula
- nht
- compound
- neamine
- carbon atoms
- Prior art date
Links
- SYJXFKPQNSDJLI-HKEUSBCWSA-N neamine Chemical compound N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](N)C[C@@H]1N SYJXFKPQNSDJLI-HKEUSBCWSA-N 0.000 title claims 38
- 238000004519 manufacturing process Methods 0.000 title 1
- XXJGBENTLXFVFI-UHFFFAOYSA-N 1-amino-methylene Chemical compound N[CH2] XXJGBENTLXFVFI-UHFFFAOYSA-N 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 4
- 230000000903 blocking effect Effects 0.000 claims description 4
- 101100006982 Mus musculus Ppcdc gene Proteins 0.000 claims description 2
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 37
- 150000001875 compounds Chemical class 0.000 claims 23
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 21
- 125000004432 carbon atom Chemical group C* 0.000 claims 19
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 18
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 12
- -1 carboxylic acid hydrocarbon radical Chemical class 0.000 claims 11
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 9
- 239000002253 acid Substances 0.000 claims 8
- 125000003277 amino group Chemical group 0.000 claims 8
- 238000010992 reflux Methods 0.000 claims 8
- QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 claims 8
- 125000002252 acyl group Chemical group 0.000 claims 6
- FQGYCXFLEQVDJQ-UHFFFAOYSA-N mercury dicyanide Chemical compound N#C[Hg]C#N FQGYCXFLEQVDJQ-UHFFFAOYSA-N 0.000 claims 6
- 238000002360 preparation method Methods 0.000 claims 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 6
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 claims 6
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims 5
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 5
- 238000005903 acid hydrolysis reaction Methods 0.000 claims 5
- 150000002148 esters Chemical class 0.000 claims 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 4
- 239000003513 alkali Substances 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 239000007864 aqueous solution Substances 0.000 claims 4
- 238000006243 chemical reaction Methods 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 239000011347 resin Substances 0.000 claims 4
- 229920005989 resin Polymers 0.000 claims 4
- HEWZVZIVELJPQZ-UHFFFAOYSA-N 2,2-dimethoxypropane Chemical compound COC(C)(C)OC HEWZVZIVELJPQZ-UHFFFAOYSA-N 0.000 claims 3
- 125000004442 acylamino group Chemical group 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000006242 amine protecting group Chemical group 0.000 claims 3
- 238000006206 glycosylation reaction Methods 0.000 claims 3
- 125000006239 protecting group Chemical group 0.000 claims 3
- 239000011541 reaction mixture Substances 0.000 claims 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- 150000001335 aliphatic alkanes Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 125000004983 dialkoxyalkyl group Chemical group 0.000 claims 2
- 230000013595 glycosylation Effects 0.000 claims 2
- 150000004820 halides Chemical class 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 2
- AOSZTAHDEDLTLQ-AZKQZHLXSA-N (1S,2S,4R,8S,9S,11S,12R,13S,19S)-6-[(3-chlorophenyl)methyl]-12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-azapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one Chemical compound C([C@@H]1C[C@H]2[C@H]3[C@]([C@]4(C=CC(=O)C=C4[C@@H](F)C3)C)(F)[C@@H](O)C[C@@]2([C@@]1(C1)C(=O)CO)C)N1CC1=CC=CC(Cl)=C1 AOSZTAHDEDLTLQ-AZKQZHLXSA-N 0.000 claims 1
- 241000251468 Actinopterygii Species 0.000 claims 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical group C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 229940126657 Compound 17 Drugs 0.000 claims 1
- OPFJDXRVMFKJJO-ZHHKINOHSA-N N-{[3-(2-benzamido-4-methyl-1,3-thiazol-5-yl)-pyrazol-5-yl]carbonyl}-G-dR-G-dD-dD-dD-NH2 Chemical compound S1C(C=2NN=C(C=2)C(=O)NCC(=O)N[C@H](CCCN=C(N)N)C(=O)NCC(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(N)=O)=C(C)N=C1NC(=O)C1=CC=CC=C1 OPFJDXRVMFKJJO-ZHHKINOHSA-N 0.000 claims 1
- 238000007171 acid catalysis Methods 0.000 claims 1
- 239000003377 acid catalyst Substances 0.000 claims 1
- RBADLHJXVXRWQY-UHFFFAOYSA-N benzene;nitromethane Chemical compound C[N+]([O-])=O.C1=CC=CC=C1 RBADLHJXVXRWQY-UHFFFAOYSA-N 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 229960003328 benzoyl peroxide Drugs 0.000 claims 1
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 229940126086 compound 21 Drugs 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical group 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 230000007062 hydrolysis Effects 0.000 claims 1
- 238000006460 hydrolysis reaction Methods 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 claims 1
- 230000037361 pathway Effects 0.000 claims 1
- 125000003652 trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/22—Cyclohexane rings, substituted by nitrogen atoms
- C07H15/222—Cyclohexane rings substituted by at least two nitrogen atoms
- C07H15/224—Cyclohexane rings substituted by at least two nitrogen atoms with only one saccharide radical directly attached to the cyclohexyl radical, e.g. destomycin, fortimicin, neamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/22—Cyclohexane rings, substituted by nitrogen atoms
- C07H15/222—Cyclohexane rings substituted by at least two nitrogen atoms
- C07H15/226—Cyclohexane rings substituted by at least two nitrogen atoms with at least two saccharide radicals directly attached to the cyclohexane rings
- C07H15/234—Cyclohexane rings substituted by at least two nitrogen atoms with at least two saccharide radicals directly attached to the cyclohexane rings attached to non-adjacent ring carbon atoms of the cyclohexane rings, e.g. kanamycins, tobramycin, nebramycin, gentamicin A2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Communicable Diseases (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Saccharide Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/611,349 US3996205A (en) | 1975-09-08 | 1975-09-08 | Aminoglycoside antibiotics and intermediates |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL192253A1 PL192253A1 (pl) | 1979-02-26 |
| PL111474B1 true PL111474B1 (en) | 1980-08-30 |
Family
ID=24448676
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1976192253A PL111474B1 (en) | 1975-09-08 | 1976-09-08 | Process for preparing novel neamine drivatives |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US3996205A (enExample) |
| JP (1) | JPS5233649A (enExample) |
| AU (1) | AU506262B2 (enExample) |
| BE (1) | BE845942A (enExample) |
| CA (1) | CA1067899A (enExample) |
| CH (1) | CH626896A5 (enExample) |
| DE (1) | DE2638794A1 (enExample) |
| FR (2) | FR2322608A1 (enExample) |
| GB (1) | GB1530643A (enExample) |
| HU (1) | HU177271B (enExample) |
| NL (1) | NL7609874A (enExample) |
| PL (1) | PL111474B1 (enExample) |
| SU (1) | SU700066A3 (enExample) |
| ZA (1) | ZA764726B (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4182855A (en) * | 1977-05-05 | 1980-01-08 | The Upjohn Company | Nitrosugar |
| US7794713B2 (en) | 2004-04-07 | 2010-09-14 | Lpath, Inc. | Compositions and methods for the treatment and prevention of hyperproliferative diseases |
| LT2390255T (lt) * | 2006-04-03 | 2016-10-25 | Technion Research & Development Foundation Ltd. | Nauji aminoglikozidai ir jų panaudojimas genetinių sutrikimų gydyme |
| US7862812B2 (en) | 2006-05-31 | 2011-01-04 | Lpath, Inc. | Methods for decreasing immune response and treating immune conditions |
| HK1257935A1 (zh) | 2015-09-02 | 2019-11-01 | Eloxx Pharmaceuticals Ltd. | 氨基糖苷衍生物及其在治疗遗传性病症中的应用 |
| EP3344640A4 (en) | 2015-09-02 | 2019-05-01 | Eloxx Pharmaceuticals Ltd. | AMINO-LIKES DERIVATIVES AND USES THEREOF FOR THE TREATMENT OF GENETIC DISEASES |
| WO2017037718A1 (en) | 2015-09-02 | 2017-03-09 | Eloxx Pharmaceuticals Ltd. | Aminoglycoside derivatives and uses thereof in treating genetic disorders |
| JP7187471B2 (ja) | 2017-03-15 | 2022-12-12 | エロックス ファーマシューティカルズ リミテッド | 擬似三糖アミノグリコシドおよびその中間体の大規模調製 |
| WO2020105054A1 (en) | 2018-11-22 | 2020-05-28 | Technion Research & Development Foundation Limited | Modified aminoglycoside compounds and uses thereof in disabling bacterial ribosome |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH84A (fr) * | 1889-01-10 | Fontainemelon Horlogerie | Perfectionnement apporté dans la construction des mécanismes de remontoir des montres de tous calibres | |
| JPS507595B1 (enExample) * | 1970-07-29 | 1975-03-27 | ||
| US3792037A (en) * | 1971-11-04 | 1974-02-12 | Bristol Myers Co | Process for preparing ambutyrosin |
| CA992535A (en) * | 1972-03-08 | 1976-07-06 | Bristol-Myers Squibb Company | Antibiotic derivatives |
| US3897412A (en) * | 1972-05-04 | 1975-07-29 | Bristol Myers Co | Paromomycin antibiotic derivatives |
| US3860574A (en) * | 1972-12-06 | 1975-01-14 | Bristol Myers Co | Derivatives of neomycin b and neomycin c |
| US3886139A (en) * | 1973-02-23 | 1975-05-27 | Bristol Myers Co | Derivatives of kanamycin |
| US3893997A (en) * | 1974-07-01 | 1975-07-08 | Smithkline Corp | Pseudodisaccharide intermediates |
-
1975
- 1975-09-08 US US05/611,349 patent/US3996205A/en not_active Expired - Lifetime
-
1976
- 1976-07-27 CA CA257,925A patent/CA1067899A/en not_active Expired
- 1976-08-05 ZA ZA764726A patent/ZA764726B/xx unknown
- 1976-08-06 AU AU16626/76A patent/AU506262B2/en not_active Expired
- 1976-08-19 GB GB34527/76A patent/GB1530643A/en not_active Expired
- 1976-08-27 DE DE19762638794 patent/DE2638794A1/de not_active Withdrawn
- 1976-09-03 JP JP51105075A patent/JPS5233649A/ja active Pending
- 1976-09-06 NL NL7609874A patent/NL7609874A/xx not_active Application Discontinuation
- 1976-09-07 SU SU762393663A patent/SU700066A3/ru active
- 1976-09-07 FR FR7626904A patent/FR2322608A1/fr active Granted
- 1976-09-08 PL PL1976192253A patent/PL111474B1/pl unknown
- 1976-09-08 BE BE170428A patent/BE845942A/xx not_active IP Right Cessation
- 1976-09-08 CH CH1140476A patent/CH626896A5/de not_active IP Right Cessation
- 1976-09-08 HU HU76UO124A patent/HU177271B/hu unknown
-
1977
- 1977-08-05 FR FR7724310A patent/FR2355852A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| US3996205A (en) | 1976-12-07 |
| NL7609874A (nl) | 1977-03-10 |
| JPS5233649A (en) | 1977-03-14 |
| AU1662676A (en) | 1978-02-09 |
| PL192253A1 (pl) | 1979-02-26 |
| FR2355852A1 (fr) | 1978-01-20 |
| DE2638794A1 (de) | 1977-03-10 |
| AU506262B2 (en) | 1979-12-20 |
| ZA764726B (en) | 1977-07-27 |
| FR2355852B1 (enExample) | 1980-04-04 |
| CA1067899A (en) | 1979-12-11 |
| FR2322608B1 (enExample) | 1979-09-07 |
| GB1530643A (en) | 1978-11-01 |
| CH626896A5 (enExample) | 1981-12-15 |
| SU700066A3 (ru) | 1979-11-25 |
| FR2322608A1 (fr) | 1977-04-01 |
| HU177271B (en) | 1981-08-28 |
| BE845942A (fr) | 1977-03-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PL111474B1 (en) | Process for preparing novel neamine drivatives | |
| EP3802556A1 (en) | Lipid-modified nucleic acid compounds and methods | |
| RU2012107130A (ru) | Композиция для нанесения металлического покрытия, содержащая подавляющий агент, для беспустотного заполнения субмикронных элементов поверхности | |
| Miyake et al. | The structures of a β-galactosidase inhibitor, galactostatin, and its derivatives | |
| JPWO2017010575A1 (ja) | β２ＧＰＩ遺伝子発現抑制核酸複合体 | |
| CH649559A5 (it) | 4'-iododerivati di glicosidi antraciclinonici. | |
| PT78938A (fr) | Procede de preparation de benzyl-phenyl-osides utiles en therapeutique | |
| KR20220150881A (ko) | 핵산 및 반감기 연장 모티프를 포함하는 화합물 | |
| ES8101622A1 (es) | Un procedimiento para la produccion de un derivado de antra-ciclina | |
| US3758455A (en) | Reof mycophenolic acid glucuronide and the process for the preparation the | |
| TW200416224A (en) | Novel 2',5'-oligoadenylic acid compositions | |
| US11639364B2 (en) | Potent sialyltransferase inhibitors | |
| Zehavi et al. | Polymers Having (1→ 4)-and (1→ 6)-linked α-d-glucopyranosyl Groups as Acceptors in the Glycogen Synthase Reaction | |
| US2642430A (en) | Hydroxy substituted aliphatic ether derivatives of nitrogen heterocyclics | |
| KR890000547A (ko) | 비개질되거나 개질된 천연 수지계 질소-함유 축합물, 이의 제조방법 및 이의 용도 | |
| Padyukova et al. | A new scheme for the synthesis of 5′-nucleotide phosphonate analogs | |
| US2792388A (en) | Process for preparing nu-monoacylated glucosamine | |
| JPH0469159B2 (enExample) | ||
| Otsuka | Synthesis of Arylated Carbohydrates and Their Application | |
| EP1395599A1 (en) | Anti-tumour anthracycline glycoside 14-sulfonic acid derivatives | |
| EP2857411B1 (en) | Method for preparing fully protection heparin pentasaccharide and intermediate thereof | |
| JPS6429393A (en) | Nucleoside analog | |
| AU641540C (en) | Anionic furanose derivatives, methods of making and using the same | |
| US4607024A (en) | Epoxypropylphosphonate salt of jesamycin and pharmaceutical composition containing same | |
| Chakravarty | I. SYNTHESIS OF DERIVATIVES OF 2, 6-DIAMINO-2, 6-DIDEOXY-D-MANNOSE AND 2-AMINO-3, 6-ANHYDRO-2-DEOXY-D-MANNOSE. II. AMINO DERIVATIVES OF STARCHES. ATTEMPTED SYNTHESIS OF 2-AMINO-3, 6-ANHYDRO-2-DEOXYAMYLOSE AND DEGRADATIVE EXPERIMENTS ON N-ACETYL AMINATED AMYLOSE |