RU2018144401A - СПОСОБ ПОЛУЧЕНИЯ Si-СОДЕРЖАЩИХ БИЦИКЛО[4.2.1]НОНА-2,4,7-ТРИЕНОВ, ПРОЯВЛЯЮЩИХ ПРОТИВООПУХОЛЕВУЮ АКТИВНОСТЬ - Google Patents
СПОСОБ ПОЛУЧЕНИЯ Si-СОДЕРЖАЩИХ БИЦИКЛО[4.2.1]НОНА-2,4,7-ТРИЕНОВ, ПРОЯВЛЯЮЩИХ ПРОТИВООПУХОЛЕВУЮ АКТИВНОСТЬ Download PDFInfo
- Publication number
- RU2018144401A RU2018144401A RU2018144401A RU2018144401A RU2018144401A RU 2018144401 A RU2018144401 A RU 2018144401A RU 2018144401 A RU2018144401 A RU 2018144401A RU 2018144401 A RU2018144401 A RU 2018144401A RU 2018144401 A RU2018144401 A RU 2018144401A
- Authority
- RU
- Russia
- Prior art keywords
- trienes
- nona
- antitumor activity
- manifesting
- producing
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/695—Silicon compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/0805—Compounds with Si-C or Si-Si linkages comprising only Si, C or H atoms
Claims (4)
1. Способ получения Si-содержащих бицикло[4.2.1]нона-2,4,7-триенов общей формулы (1):
каталитическим взаимодействием 1,3,5-циклогептатриена с Si-содержащими алкинами в присутствии каталитической системы Ti(acac)2Cl2-Et2AlCl, отличающийся тем, что, в качестве 1,3,5-циклогептатриена используют 1-метил(пропил)циклогепта-1,3,5-триен, реакцию 1-метил(пропил)циклогепта-1,3,5-триена (ЦГТ) с Si-содержащим алкином общей формулы (где R - указанные выше) проводят при мольном соотношении Si-содержащий алкин : ЦГТ : Ti(acac)2Cl2 : Et2AlCl = (1.7-2.4):2:(0.05-0.2):2, в ампуле при 20-120°С, в бензоле в течение 8-48 ч.
2. Применение Si-содержащих бицикло[4.2.1]нона-2,4,7-триенов в качестве средств с противоопухолевой активностью.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
RU2018144401A RU2726195C2 (ru) | 2018-12-14 | 2018-12-14 | СПОСОБ ПОЛУЧЕНИЯ Si-СОДЕРЖАЩИХ БИЦИКЛО[4.2.1]НОНА-2,4,7-ТРИЕНОВ, ПРОЯВЛЯЮЩИХ ПРОТИВООПУХОЛЕВУЮ АКТИВНОСТЬ |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
RU2018144401A RU2726195C2 (ru) | 2018-12-14 | 2018-12-14 | СПОСОБ ПОЛУЧЕНИЯ Si-СОДЕРЖАЩИХ БИЦИКЛО[4.2.1]НОНА-2,4,7-ТРИЕНОВ, ПРОЯВЛЯЮЩИХ ПРОТИВООПУХОЛЕВУЮ АКТИВНОСТЬ |
Publications (3)
Publication Number | Publication Date |
---|---|
RU2018144401A3 RU2018144401A3 (ru) | 2020-06-15 |
RU2018144401A true RU2018144401A (ru) | 2020-06-15 |
RU2726195C2 RU2726195C2 (ru) | 2020-07-09 |
Family
ID=71095400
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2018144401A RU2726195C2 (ru) | 2018-12-14 | 2018-12-14 | СПОСОБ ПОЛУЧЕНИЯ Si-СОДЕРЖАЩИХ БИЦИКЛО[4.2.1]НОНА-2,4,7-ТРИЕНОВ, ПРОЯВЛЯЮЩИХ ПРОТИВООПУХОЛЕВУЮ АКТИВНОСТЬ |
Country Status (1)
Country | Link |
---|---|
RU (1) | RU2726195C2 (ru) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2551278C1 (ru) * | 2013-11-06 | 2015-05-20 | Федеральное государственное бюджетное учреждение науки Институт нефтехимии и катализа Российской академии наук | Способ получения бицикло[4.2.1]нона-2,4-диенов |
RU2541530C1 (ru) * | 2013-11-18 | 2015-02-20 | Федеральное государственное бюджетное учреждение науки Институт нефтехимии и катализа Российской академии наук | СПОСОБ ПОЛУЧЕНИЯ Si-СОДЕРЖАЩИХ БИС-(ЭНДО-БИЦИКЛО[4.2.1]НОНА-2,4,7-ТРИЕНОВ) |
RU2559365C2 (ru) * | 2013-11-18 | 2015-08-10 | Федеральное государственное бюджетное учреждение науки Институт нефтехимии и катализа Российской академии наук | СПОСОБ ПОЛУЧЕНИЯ Si-СОДЕРЖАЩИХ БИЦИКЛО[4.2.1]НОНА-2,4,7-ТРИЕНОВ |
-
2018
- 2018-12-14 RU RU2018144401A patent/RU2726195C2/ru not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
RU2726195C2 (ru) | 2020-07-09 |
RU2018144401A3 (ru) | 2020-06-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Le Bailly et al. | Iron-catalysed reduction of carbonyls and olefins | |
Lee et al. | Lewis base activation of grignard reagents with N-heterocyclic carbenes. Cu-free catalytic enantioselective additions to γ-chloro-α, β-unsaturated esters | |
Gomez-Gallego et al. | Kinetic isotope effects in the study of organometallic reaction mechanisms | |
Gomez-Suarez et al. | Influence of a very bulky N-heterocyclic carbene in gold-mediated catalysis | |
Lee et al. | Highly site-and enantioselective Cu-catalyzed allylic alkylation reactions with easily accessible vinylaluminum reagents | |
Volla et al. | Iron-catalyzed desulfinylative CC cross-coupling reactions of sulfonyl chlorides with Grignard reagents | |
Agrawal et al. | Iron-catalyzed coupling of aryl sulfamates and aryl/vinyl tosylates with aryl Grignards | |
Oelerich et al. | DNA-based asymmetric organometallic catalysis in water | |
Yi et al. | The ruthenium acetylide catalyzed cross-coupling reaction of terminal and internal alkynes: isolation of a catalytically active β-agostic intermediate species | |
Cabrita et al. | Reduction of sulfoxides catalyzed by oxo-complexes | |
Cheng et al. | Iridium-catalyzed asymmetric ring-opening of oxabenzonorbornadienes with phenols | |
Lane et al. | The iron-catalyzed construction of 2-aminopyrimidines from alkynenitriles and cyanamides | |
Smirnov et al. | Photoredox generation of the trifluoromethyl radical from borate complexes via single electron reduction | |
McKeown et al. | Platinum (II)-catalyzed ethylene hydrophenylation: switching selectivity between alkyl-and vinylbenzene production | |
Darcel et al. | Iron-catalyzed reduction and hydroelementation reactions | |
Ohashi et al. | Preparation of Trifluorovinyl Compounds by Lithium Salt-promoted Monoalkylation of Tetrafluoroethene | |
RU2017100437A (ru) | Комплексы | |
Komeyama et al. | Nickel-Catalyzed Reductive Bis-Allylation of Alkynes | |
RU2018144401A (ru) | СПОСОБ ПОЛУЧЕНИЯ Si-СОДЕРЖАЩИХ БИЦИКЛО[4.2.1]НОНА-2,4,7-ТРИЕНОВ, ПРОЯВЛЯЮЩИХ ПРОТИВООПУХОЛЕВУЮ АКТИВНОСТЬ | |
Schomaker et al. | Cobalt Dinitrosoalkane Complexes in the C− H Functionalization of Olefins | |
Sasaki et al. | Iridium (I)‐catalyzed C− H Borylation of α, β‐Unsaturated Esters with Bis (pinacolato) diboron | |
Sokol et al. | Catalytic platinum-initiated cation-olefin reactions with alkene terminating groups | |
Hirano et al. | Stoichiometric and Catalytic Cross Dimerization between Conjugated Dienes and Conjugated Carbonyls by a Ruthenium (0) Complex: Straightforward Access to Unsaturated Carbonyl Compounds by an Oxidative Coupling Mechanism | |
Fuentes et al. | Intermetallic coinage metal-catalyzed functionalization of alkanes with ethyl diazoacetate: Gold as a ligand | |
Graham et al. | Regioselective semihydrogenation of dienes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | The patent is invalid due to non-payment of fees |
Effective date: 20201215 |