(-)-SCLAREOL CONVERSION IN RITTER'S REACTION CONDITIONS
The main products of sclareol (1) Ritter’s reaction in mild conditions are (8R,13R)-Labd-14(15)-en-8,13-diacetamide (2) (8R,13S)-Labd-14(15)-en-8,13-diacetamide (3) stereoisomeric on C13 atom and having unrearranged native diol skeleton. We present in the current communication the results of sclareo...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
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Academy of Sciences of Moldova, Institute of Chemistry
2012-12-01
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| Series: | Chemistry Journal of Moldova: General, Industrial and Ecological Chemistry |
| Subjects: | |
| Online Access: | http://www.cjm.asm.md/sites/default/files/article_files/Kovalskaia%20147-148.pdf |
| _version_ | 1819149397737340928 |
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| author | S. Kovalskaya N. Kozlov A. Aricu V. Kulcitki N. Ungur |
| author_facet | S. Kovalskaya N. Kozlov A. Aricu V. Kulcitki N. Ungur |
| author_sort | S. Kovalskaya |
| collection | DOAJ |
| description | The main products of sclareol (1) Ritter’s reaction in mild conditions are (8R,13R)-Labd-14(15)-en-8,13-diacetamide (2) (8R,13S)-Labd-14(15)-en-8,13-diacetamide (3) stereoisomeric on C13 atom and having unrearranged native diol skeleton. We present in the current communication the results of sclareol converting (1) into nitrogen-containing labdanes
in the Ritter’s reaction conditions. |
| first_indexed | 2024-12-22T14:00:58Z |
| format | Article |
| id | doaj.art-1b7a69356dca42cd8a8fcd11d027a528 |
| institution | Directory Open Access Journal |
| issn | 1857-1727 2345-1688 |
| language | English |
| last_indexed | 2024-12-22T14:00:58Z |
| publishDate | 2012-12-01 |
| publisher | Academy of Sciences of Moldova, Institute of Chemistry |
| record_format | Article |
| series | Chemistry Journal of Moldova: General, Industrial and Ecological Chemistry |
| spelling | doaj.art-1b7a69356dca42cd8a8fcd11d027a5282022-12-21T18:23:25ZengAcademy of Sciences of Moldova, Institute of ChemistryChemistry Journal of Moldova: General, Industrial and Ecological Chemistry1857-17272345-16882012-12-0172147148(-)-SCLAREOL CONVERSION IN RITTER'S REACTION CONDITIONS S. Kovalskaya0N. Kozlov1A. Aricu2V. Kulcitki3N. Ungur4 Institute of Physical Organic Chemistry, National Academy of Sciences of Belarus Institute of Physical Organic Chemistry, National Academy of Sciences of BelarusInstitute of Chemistry of Academy of Sciences of MoldovaInstitute of Chemistry of Academy of Sciences of MoldovaInstitute of Chemistry of Academy of Sciences of MoldovaThe main products of sclareol (1) Ritter’s reaction in mild conditions are (8R,13R)-Labd-14(15)-en-8,13-diacetamide (2) (8R,13S)-Labd-14(15)-en-8,13-diacetamide (3) stereoisomeric on C13 atom and having unrearranged native diol skeleton. We present in the current communication the results of sclareol converting (1) into nitrogen-containing labdanes in the Ritter’s reaction conditions.http://www.cjm.asm.md/sites/default/files/article_files/Kovalskaia%20147-148.pdfMALDI-ToFX-ray phase analysisalbuminimmunoglobulin Ghydroxyapatiteinteraction. |
| spellingShingle | S. Kovalskaya N. Kozlov A. Aricu V. Kulcitki N. Ungur (-)-SCLAREOL CONVERSION IN RITTER'S REACTION CONDITIONS Chemistry Journal of Moldova: General, Industrial and Ecological Chemistry MALDI-ToF X-ray phase analysis albumin immunoglobulin G hydroxyapatite interaction. |
| title | (-)-SCLAREOL CONVERSION IN RITTER'S REACTION CONDITIONS |
| title_full | (-)-SCLAREOL CONVERSION IN RITTER'S REACTION CONDITIONS |
| title_fullStr | (-)-SCLAREOL CONVERSION IN RITTER'S REACTION CONDITIONS |
| title_full_unstemmed | (-)-SCLAREOL CONVERSION IN RITTER'S REACTION CONDITIONS |
| title_short | (-)-SCLAREOL CONVERSION IN RITTER'S REACTION CONDITIONS |
| title_sort | sclareol conversion in ritter s reaction conditions |
| topic | MALDI-ToF X-ray phase analysis albumin immunoglobulin G hydroxyapatite interaction. |
| url | http://www.cjm.asm.md/sites/default/files/article_files/Kovalskaia%20147-148.pdf |
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