Zobrazeno 1 - 10
of 30
pro vyhledávání: '"V. N. Karel'skii"'
Publikováno v:
Chemistry of Natural Compounds. 16:282-286
A new scheme for the synthesis of a peptide representing a modified analog of fragments 13–19 of the sequence of the adrenocorticotropic hormone has been described, which uses a number of stages the trimethylsilyl grouping for the protection of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc9d178a319af2ce1d2f54bcc850ad92
https://doi.org/10.1007/bf00567293
https://doi.org/10.1007/bf00567293
Publikováno v:
Chemistry and Technology of Fuels and Oils. 13:545-548
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffe3e3c138340affb22cd78d2d5966c8
https://doi.org/10.1007/bf00719081
https://doi.org/10.1007/bf00719081
Publikováno v:
Chemistry and Technology of Fuels and Oils. 15:220-223
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::986db93a48490e80a2f4213ab4acaaa7
https://doi.org/10.1007/bf00723451
https://doi.org/10.1007/bf00723451
Autor:
V. M. Shkol'nikov, V. D. Milovanov, Yu. N. Shekhter, V. N. Karel'skii, G. G. Kotova, L. D. Shishkina
Publikováno v:
Chemistry and Technology of Fuels and Oils. 13:171-174
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5189897fbfcdb5ecd7a8907bc553b240
https://doi.org/10.1007/bf00729321
https://doi.org/10.1007/bf00729321
Publikováno v:
Chemistry of Natural Compounds. 21:520-523
A new variant of the preparative synthesis of hexapeptide 11–16 of the natural sequence of human calcitonin is described. In several of the stages 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline was used successfully as the condensing agent. The fin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c92fcf7ec1c991caeb97a2e01a784b7
https://doi.org/10.1007/bf00579150
https://doi.org/10.1007/bf00579150
Publikováno v:
Chemistry of Natural Compounds. 23:746-751
A mixture of peptides containing 30.4% of oxytocin has been obtained by the solid-phase method on the benzhydrylamine resin UR-95. A procedure is given for the quantitative determination of oxytocin in a mixture of peptides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d173efdc629f1386faab1e3e64d888c5
https://doi.org/10.1007/bf00596659
https://doi.org/10.1007/bf00596659
Publikováno v:
Chemistry of Natural Compounds. 15:324-328
The paper gives the results of the synthesis of the tripeptide arginyl-arginylproline performed with the use of various condensing agents. Nα-tert-Butoxycarbonyl-Nω-nitroarginine was used as the starting compound. Some physicochemical characteristi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f65761a969bee3595e5af407589ee50
https://doi.org/10.1007/bf00566085
https://doi.org/10.1007/bf00566085
Publikováno v:
Chemistry of Natural Compounds. 18:90-94
The results are given of the synthesis of the heptapeptide 13–19 of the natural sequence of ACTH using, in a number of stages, the pentafluorophyl esters of amino acids and peptides in combination with the temporary silyl protection of the carboxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01917a911385fdfca5fea0a873e6e74a
https://doi.org/10.1007/bf00581604
https://doi.org/10.1007/bf00581604
Publikováno v:
Pharmaceutical Chemistry Journal. 14:410-413
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96c7128670477b2f58a45a7394005dce
https://doi.org/10.1007/bf00780189
https://doi.org/10.1007/bf00780189
Publikováno v:
Chemistry of Natural Compounds. 22:706-709
A scheme is given for the synthesis of a heptapeptide representing a modified ACTH 4–10 fragment on the basis of which it is possible to create a preparation that is an effective adaptogen of peptide nature. A proposed variant of the synthesis perm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::458b5cc68e1543e62decdc64c1c04046
https://doi.org/10.1007/bf00598358
https://doi.org/10.1007/bf00598358