FIELD: chemistry.
SUBSTANCE: invention relates to field of organic chemistry, namely to method of obtaining functionally substituted fullerenes, which can be applied as highly active initial substances in synthesis of medications of new generation for treatment of dangerous human diseases. method of selective obtaining of 1'-alkyl-1'-N- cyclohexylcarboxaamidylcyclopropa[2',3':1,9](C60-Ih)[5,6]fullerenes (1) is realised due to interaction of C60-fullerene with α-substituted diazoamides of formula N2C(R)C(O)NHCy (R=Me, i-Bu, -(CH2)2SMe) in o-dichlorobenzene in presence of three-component catalyst {Pd(acac)2:2PPh3:4Et3Al}, taken in molar ratio C60:diazocompound:Pd(acac)2:PPh3:Et3Al=0.01:(0.03-0.07):(0.0015-0.0025):(0.003-0.005):(0.006-0.01) Interaction is performed at temperature 80°C for 0.2-1.0 h.
EFFECT: selective obtaining of 1'-alkyl-1'-N- cyclohexylcarboxaamidylcyclopropa[2',3':1,9](C60-Ih)[5,6]fullerenes .
1 tbl
Title | Year | Author | Number |
---|---|---|---|
METHOD FOR COMBINED SYNTHESIS OF 1'-[2-(METHYLSULPHANYL)ETHYL]-1'-ETHYLFORMYL-(C-I)[5,6]FULLERO[2',3':1,9]CYCLOPROPANE AND 1'a-[2-(METHYLSULPHANYL)ETHYL]-1'a-ETHYLFORMYL -1'a-CARBA-1'(2')a-HOMO(C-I)[5,6]FULLERENE | 2008 |
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METHOD FOR COMBINED SYNTHESIS OF 1'-(3-1H-INDOLEMETHYL)-1'-ETHYLFORMYL-(C-I)[5,6]FULLERO[2'3':1,9]CYCLOPROPANE AND 1'a-(3-1H-INDOLEMETHYL)1'a-ETHYLFORMYL-1'a-CARBA-1'(2')a-HOMO(C-I)[5,6]FULLERENE | 2008 |
|
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METHOD FOR SELECTIVE SYNTHESIS OF 1'-[2-METHYLSULPHANYL)-ETHYL]-1'-ETHYLFORMYLCYCLOPROPA [2'3':1,9] (C-I) [5,6] FULLERENE | 2010 |
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METHOD OF PRODUCING 1a-METHYL-1a-(3'-THIOALKYLPROP-2'-YL)-1aH-1(9)a-homo(C-I)[5,6]FULLERENES | 2010 |
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RU2434839C2 |
METHOD FOR COMBINED PRODUCTION OF 1'-ETHYLFORMYL-(C-I)[5,6]FULLERO [2',3':1,9]CYCLOPROPANE AND 1'a-ETHYLFORMYL-1'a-CARBA-1'(2')a-HOMO(C-I)[5,6]FULLERENE | 2008 |
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METHOD OF PRODUCING CYCLOALKYLIDENEHOMO(C-C)[5,6]FULLERENE | 2009 |
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RU2417980C2 |
METHOD OF PRODUCING N-ALKYL AND N-ARYLCARBOXAMIDYL-1aH,2'H-[1,2]PYRAZOLINO[3',4':1,9](C-I)-[5,6]FULLERENES | 2012 |
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RU2517170C2 |
Authors
Dates
2015-01-27—Published
2013-02-05—Filed