Zobrazeno 1 - 10
of 10
pro vyhledávání: '"A. S. Gapoyan"'
Publikováno v:
Russian Chemical Reviews. 54:262-276
The methods of synthesis and the chemical and biological properties of furo-, thieno-, and pyrrolo-[2,3-d]pyrimidines are described. The bibliography includes 201 references.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fca97595cce18508c4eb9a6d955e2577
https://doi.org/10.1070/rc1985v054n03abeh003026
https://doi.org/10.1070/rc1985v054n03abeh003026
Publikováno v:
Chemistry of Heterocyclic Compounds. 21:572-575
A number of aldimines of 7-aminopyrrolo[2,3-d]pyrimidine have been synthesized by the action of bromine on hydrazones of 5-allyl-4-hydrazinopyridine. The structures of the compounds obtained were confirmed by IR spectroscopy and mass spectrometry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10fc21ef206eefc1cd3569d126ff25a4
https://doi.org/10.1007/bf00506076
https://doi.org/10.1007/bf00506076
Publikováno v:
Chemistry of Heterocyclic Compounds. 18:1305-1308
The action of bromine on 5-allyl-6-aminopyrimidines was studied. The formation of both a product of addition of bromine to the allylic bond and pyrrolo [2,3-d]-pyrimidines is possible, depending on the character of the substituent attached to the ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0880772c62279f879b4fc8a6b9eb732f
https://doi.org/10.1007/bf00506623
https://doi.org/10.1007/bf00506623
Publikováno v:
Chemistry of Heterocyclic Compounds. 18:100-102
A new scheme was developed for the synthesis of 2,4-dimethy1-5,6-dihydro-6-bromomethylthieno[2,3-d]pyrimidine by bromination of the corresponding 5-allyl-6-mercaptopyrimidine. It is shown that when the bromomethyl derivative is treated with sodium me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::042f1b20c98ef722311dcf204e5018ae
https://doi.org/10.1007/bf00513299
https://doi.org/10.1007/bf00513299
Publikováno v:
Chemischer Informationsdienst. 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99a74724d5fa8705cb5db6aacfac9fe2
https://doi.org/10.1002/chin.198526389
https://doi.org/10.1002/chin.198526389
Publikováno v:
Chemischer Informationsdienst. 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::beddc8175d7ad656553f491d8634fb0c
https://doi.org/10.1002/chin.198540202
https://doi.org/10.1002/chin.198540202
Publikováno v:
Chemischer Informationsdienst. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e82385ee61b977262db53ba4c94afb79
https://doi.org/10.1002/chin.198224249
https://doi.org/10.1002/chin.198224249
Publikováno v:
Chemischer Informationsdienst. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bcde7f32e7897381be820828f3e3a45
https://doi.org/10.1002/chin.198320223
https://doi.org/10.1002/chin.198320223
Publikováno v:
Chemischer Informationsdienst. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5236025206643408ed116cdd8163ecbc
https://doi.org/10.1002/chin.198320222
https://doi.org/10.1002/chin.198320222
Publikováno v:
Pharmaceutical Chemistry Journal. 16:888-889
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3dc1c1c9d0eb37e76119a2d175edf8e
https://doi.org/10.1007/bf00767844
https://doi.org/10.1007/bf00767844