Zobrazeno 1 - 10
of 143
pro vyhledávání: '"M. G. Safarov"'
Autor:
Sh. M. Salikhov, I. M. Biktagirov, Farid A. Valeev, L. Kh. Faizullina, M. G. Safarov, F. Z. Galin
Publikováno v:
Russian Journal of Organic Chemistry. 52:711-720
Diels-Alder adducts of levoglucosenone with 1,3-butadiene, piperylene, and isoprene, and also some of their derivatives undergo allylic oxidation with CrО3·2Py only in the case when the effect of a keto group or of another electron-acceptor group i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c15933b2bbbeec03a5bf9e911b242c3
https://doi.org/10.1134/s107042801605016x
https://doi.org/10.1134/s107042801605016x
Publikováno v:
Russian Journal of Organic Chemistry. 51:1457-1463
Vicinal hydroxylation of the Diels-Alder adducts of levoglucosenone with buta-1,3-diene, penta- 1,3-diene, and cyclopentadiene by the action of sodium periodate or ozonolysis is accompanied by cleavage of the double bond, and intramolecular aldol rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f07b9789c3a4c7ef95b0b7844c59cc0
https://doi.org/10.1134/s1070428015100188
https://doi.org/10.1134/s1070428015100188
Autor:
Sh. M. Salikhov, L. Kh. Faizullina, M. G. Safarov, F. Z. Galin, M. M. Iskakova, I. M. Biktagirov, Farid A. Valeev
Publikováno v:
Russian Journal of Organic Chemistry. 51:576-581
Epoxidation of diastereoisomeric benzyloxy derivatives of the levoglucosenone adduct with cyclopentadiene by treatment with m-chloroperoxybenzoic acid afforded a mixture of 1,2- and 1,4-epoxy derivatives. Intramolecular cyclization of the hydroxy der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bae0530cb2b64f677235de279baed468
https://doi.org/10.1134/s1070428015040193
https://doi.org/10.1134/s1070428015040193
Publikováno v:
Russian Journal of Organic Chemistry. 50:1317-1322
4,4-Dimethyl-3-nitro-10,11-dioxatricyclo[6.2.1.02,6]undec-5-en-7-one possessing a bicyclic iridoid skeleton was synthesized in two steps from isolevoglucosenone which was obtained in turn from levoglucosenone through 4-benzyloxy-2-tosyloxy derivative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92d2ebcbe60955865f60c5f8a08bbb4b
https://doi.org/10.1134/s107042801409140
https://doi.org/10.1134/s107042801409140
Autor:
I. M. Biktagirov, M. M. Iskakova, Sh. M. Salikhov, Farid A. Valeev, L. Kh. Faizullina, M. G. Safarov
Publikováno v:
Russian Journal of Organic Chemistry. 50:105-109
The Dieckmann condensation of 3,4-bis(methoxycarbonylmethyl) levoglucosenone derivative afforded two regioisomeric 9,11-dioxatricyclo[6.2.1.02,6]undecane derivatives at a ratio of 5: 3. The products can be used in the synthesis of iridoids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b7f81a7897a5b46e75468d8eec189e3
https://doi.org/10.1134/s1070428014010205
https://doi.org/10.1134/s1070428014010205
Autor:
M. G. Safarov, Farid A. Valeev, Sh. M. Salikhov, A. A. Pershin, M. M. Iskakova, L. Kh. Faizullina
Publikováno v:
Russian Journal of Organic Chemistry. 48:456-459
2,2-Bis(nitromethyl)decane and 4-methyl-2,2-bis(nitromethyl)pentane reacted with α-bromolevoglucosenone in the presence of a base under ultrasonic treatment to give the corresponding cyclopenta-fused derivatives. Analogous reactions of 1,1-bis(nitro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18da02fffa73af708a036c44fe302016
https://doi.org/10.1134/s1070428012030219
https://doi.org/10.1134/s1070428012030219
Publikováno v:
Russian Journal of Organic Chemistry. 47:1750-1754
The possibility was studied of using levoglycosenone in the synthesis of N-(glucosen-2-yl) aminides. New glucosaminides were obtained containing the residues of L-a, isopinocampheol, borneol,, and (-)-(1S,2R,3S,7S,8R)-4,4-dimethyl-3-nitro-9,11-dioxat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd8d6c9affdcfb5c48a538da2412fea0
https://doi.org/10.1134/s1070428011110182
https://doi.org/10.1134/s1070428011110182
Autor:
Yu. A. Kondrova, M. G. Safarov, V. S. Kolosnitsyn, Farid A. Valeev, L. Kh. Faizullina, Leonid V. Spirikhin
Publikováno v:
Russian Journal of Organic Chemistry. 47:914-919
Michael reactions of levoglucosenone and its α-bromo and α-iodo derivatives with α,ω-dinitroalkanes were studied under conditions of chemical and electrochemical generation of base. Procedures were developed for stereospecific fusion of a cyclope
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7125c8f317b9e1340bab251a993638f7
https://doi.org/10.1134/s1070428011060145
https://doi.org/10.1134/s1070428011060145
Autor:
O. V. Shitikova, L. Kh. Kalimullina, Inna P. Tsypysheva, Farid A. Valeev, Sh. M. Salikhov, M. G. Safarov
Publikováno v:
Chemistry of Natural Compounds. 40:521-525
2-Amino derivatives of levoglucosenone were prepared by reaction of the 2-methanesulfonyl (or p-toluenesulfonyl) derivatives with ammonia, methylamine, or octylamine under various conditions. The analogous reaction did not occur for saturated derivat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::419fcf9dc4e2992ec156e926e9f26324
https://doi.org/10.1007/s10600-005-0052-8
https://doi.org/10.1007/s10600-005-0052-8
Autor:
L. Kh. Kalimullina, O. V. Shitikova, M. G. Safarov, E. V. Gorobets, Mansur S. Miftakhov, Farid A. Valeev, G. Sh. Singizova, Inna P. Tsypysheva
Publikováno v:
Chemistry of Natural Compounds. 39:563-568
Regiospecific C55 -halogenation with retention of configuration occurred upon Beckman fragmentation of levoglucosenone oxime using SOCl2 or PBr3. On the other hand, the oxime of its dihydro derivative gave under these conditions the C6 - substitution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e91016417039687f1b28b59acb3e480
https://doi.org/10.1023/b:conc.0000018110.36123.f2
https://doi.org/10.1023/b:conc.0000018110.36123.f2