Synthesis and easy intramolecular cyclization in a number of aspartyl derivatives of histamine
A series of natural and novel aspartyl derivatives of histamine were obtained by the classical peptide chemistry methods in a solution. During the synthesis of Nacetylaspartylhistamine easy and spontaneously cyclization of the protected Ac-AspOBzl into succinimide derivative was observed even after...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
MIREA - Russian Technological University
2006-08-01
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| Series: | Тонкие химические технологии |
| Online Access: | https://www.finechem-mirea.ru/jour/article/view/1425 |
| _version_ | 1797882238716608512 |
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| author | G. A. Zheltukhina E. I. Efimova T. A. Kromova V. E. Nebolsin |
| author_facet | G. A. Zheltukhina E. I. Efimova T. A. Kromova V. E. Nebolsin |
| author_sort | G. A. Zheltukhina |
| collection | DOAJ |
| description | A series of natural and novel aspartyl derivatives of histamine were obtained by the classical peptide chemistry methods in a solution. During the synthesis of Nacetylaspartylhistamine easy and spontaneously cyclization of the protected Ac-AspOBzl into succinimide derivative was observed even after one day storage. |
| first_indexed | 2024-04-10T03:32:50Z |
| format | Article |
| id | doaj.art-434b2f29d8f44df9a3d646673ea7d521 |
| institution | Directory Open Access Journal |
| issn | 2410-6593 2686-7575 |
| language | Russian |
| last_indexed | 2024-04-10T03:32:50Z |
| publishDate | 2006-08-01 |
| publisher | MIREA - Russian Technological University |
| record_format | Article |
| series | Тонкие химические технологии |
| spelling | doaj.art-434b2f29d8f44df9a3d646673ea7d5212023-03-13T07:25:27ZrusMIREA - Russian Technological UniversityТонкие химические технологии2410-65932686-75752006-08-011439431420Synthesis and easy intramolecular cyclization in a number of aspartyl derivatives of histamineG. A. Zheltukhina0E. I. Efimova1T. A. Kromova2V. E. Nebolsin3M.V. Lomonosov Moscow State University of Fine Chemical Technologies, 86, Vernadskogo pr., Moscow 119571M.V. Lomonosov Moscow State University of Fine Chemical Technologies, 86, Vernadskogo pr., Moscow 119571ООО «Фарминтерпрайсез»ООО «Фарминтерпрайсез»A series of natural and novel aspartyl derivatives of histamine were obtained by the classical peptide chemistry methods in a solution. During the synthesis of Nacetylaspartylhistamine easy and spontaneously cyclization of the protected Ac-AspOBzl into succinimide derivative was observed even after one day storage.https://www.finechem-mirea.ru/jour/article/view/1425 |
| spellingShingle | G. A. Zheltukhina E. I. Efimova T. A. Kromova V. E. Nebolsin Synthesis and easy intramolecular cyclization in a number of aspartyl derivatives of histamine Тонкие химические технологии |
| title | Synthesis and easy intramolecular cyclization in a number of aspartyl derivatives of histamine |
| title_full | Synthesis and easy intramolecular cyclization in a number of aspartyl derivatives of histamine |
| title_fullStr | Synthesis and easy intramolecular cyclization in a number of aspartyl derivatives of histamine |
| title_full_unstemmed | Synthesis and easy intramolecular cyclization in a number of aspartyl derivatives of histamine |
| title_short | Synthesis and easy intramolecular cyclization in a number of aspartyl derivatives of histamine |
| title_sort | synthesis and easy intramolecular cyclization in a number of aspartyl derivatives of histamine |
| url | https://www.finechem-mirea.ru/jour/article/view/1425 |
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