(-)-SCLAREOL CONVERSION IN RITTER'S REACTION CONDITIONS

(-)-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...

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Main Authors: S. Kovalskaya, N. Kozlov, A. Aricu, V. Kulcitki, N. Ungur
Format: Article
Language:English
Published: Academy of Sciences of Moldova, Institute of Chemistry 2012-12-01
Series:Chemistry Journal of Moldova: General, Industrial and Ecological Chemistry
Subjects:
MALDI-ToF
X-ray phase analysis
albumin
immunoglobulin G
hydroxyapatite
interaction.
Online Access:http://www.cjm.asm.md/sites/default/files/article_files/Kovalskaia%20147-148.pdf
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spelling doaj-1b7a69356dca42cd8a8fcd11d027a5282021-07-02T02:01:41ZengAcademy 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.
collection DOAJ
language English
format Article
sources DOAJ
author S. Kovalskaya
N. Kozlov
A. Aricu
V. Kulcitki
N. Ungur
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.
author_facet S. Kovalskaya
N. Kozlov
A. Aricu
V. Kulcitki
N. Ungur
author_sort S. Kovalskaya
title (-)-SCLAREOL CONVERSION IN RITTER'S REACTION CONDITIONS
title_short (-)-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_sort (-)-sclareol conversion in ritter's reaction conditions
publisher Academy of Sciences of Moldova, Institute of Chemistry
series Chemistry Journal of Moldova: General, Industrial and Ecological Chemistry
issn 1857-1727
2345-1688
publishDate 2012-12-01
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.
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
work_keys_str_mv AT skovalskaya sclareolconversioninrittersreactionconditions
AT nkozlov sclareolconversioninrittersreactionconditions
AT aaricu sclareolconversioninrittersreactionconditions
AT vkulcitki sclareolconversioninrittersreactionconditions
AT nungur sclareolconversioninrittersreactionconditions
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