One-step Selective Synthesis of 13-epi-manoyl Oxide
The selective one-step synthesis of 13-epi-manoyl oxide is reported based on a low-temperature superacidic cyclization of sclareol. The reaction conditions have been finely tuned in order to achieve a 9:1 ratio between epimeric oxides in favor of the desired 13-epi-oxide.
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Academy of Sciences of Moldova, Institute of Chemistry
2021-07-01
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Series: | Chemistry Journal of Moldova: General, Industrial and Ecological Chemistry |
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http://www.cjm.asm.md/sites/default/files/article_files/ChemJMold_10.19261cjm.2021.820-Kulcitki.pdf
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doaj-fe9885feccab43f8b2b1936d67131a1f2021-07-05T16:22:45ZengAcademy of Sciences of Moldova, Institute of ChemistryChemistry Journal of Moldova: General, Industrial and Ecological Chemistry1857-17272345-16882021-07-011619910410.19261/cjm.2021.820820One-step Selective Synthesis of 13-epi-manoyl OxideOlga Morarescu0Marionela Traistari1Alic Barba2Gheorghe Duca3Nicon Ungur4Veaceslav Kulcițki5 Institute of Chemistry, 3, Academiei str., Chisinau MD-2028, Republic of Moldova Moldova State University, 60, Mateevici str., Chisinau MD-2009, Republic of Moldova Institute of Chemistry, 3, Academiei str., Chisinau MD-2028, Republic of Moldova Institute of Chemistry, 3, Academiei str., Chisinau MD-2028, Republic of Moldova Institute of Chemistry, 3, Academiei str., Chisinau MD-2028, Republic of Moldova Institute of Chemistry, 3, Academiei str., Chisinau MD-2028, Republic of Moldova The selective one-step synthesis of 13-epi-manoyl oxide is reported based on a low-temperature superacidic cyclization of sclareol. The reaction conditions have been finely tuned in order to achieve a 9:1 ratio between epimeric oxides in favor of the desired 13-epi-oxide. http://www.cjm.asm.md/sites/default/files/article_files/ChemJMold_10.19261cjm.2021.820-Kulcitki.pdf sclareolcyclizationsuperacidetherlabdane |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Olga Morarescu Marionela Traistari Alic Barba Gheorghe Duca Nicon Ungur Veaceslav Kulcițki |
spellingShingle |
Olga Morarescu Marionela Traistari Alic Barba Gheorghe Duca Nicon Ungur Veaceslav Kulcițki One-step Selective Synthesis of 13-epi-manoyl Oxide Chemistry Journal of Moldova: General, Industrial and Ecological Chemistry sclareol cyclization superacid ether labdane |
author_facet |
Olga Morarescu Marionela Traistari Alic Barba Gheorghe Duca Nicon Ungur Veaceslav Kulcițki |
author_sort |
Olga Morarescu |
title |
One-step Selective Synthesis of 13-epi-manoyl Oxide |
title_short |
One-step Selective Synthesis of 13-epi-manoyl Oxide |
title_full |
One-step Selective Synthesis of 13-epi-manoyl Oxide |
title_fullStr |
One-step Selective Synthesis of 13-epi-manoyl Oxide |
title_full_unstemmed |
One-step Selective Synthesis of 13-epi-manoyl Oxide |
title_sort |
one-step selective synthesis of 13-epi-manoyl oxide |
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 |
2021-07-01 |
description |
The selective one-step synthesis of 13-epi-manoyl oxide is reported based on a low-temperature superacidic cyclization of sclareol. The reaction conditions have been finely tuned in order to achieve a 9:1 ratio between epimeric oxides in favor of the desired 13-epi-oxide. |
topic |
sclareol cyclization superacid ether labdane |
url |
http://www.cjm.asm.md/sites/default/files/article_files/ChemJMold_10.19261cjm.2021.820-Kulcitki.pdf
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work_keys_str_mv |
AT olgamorarescu onestepselectivesynthesisof13epimanoyloxide AT marionelatraistari onestepselectivesynthesisof13epimanoyloxide AT alicbarba onestepselectivesynthesisof13epimanoyloxide AT gheorgheduca onestepselectivesynthesisof13epimanoyloxide AT niconungur onestepselectivesynthesisof13epimanoyloxide AT veaceslavkulcitki onestepselectivesynthesisof13epimanoyloxide |
_version_ |
1721318470002409472 |