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.

Bibliographic Details
Main Authors: Olga Morarescu, Marionela Traistari, Alic Barba, Gheorghe Duca, Nicon Ungur, Veaceslav Kulcițki
Format: Article
Language:English
Published: Academy of Sciences of Moldova, Institute of Chemistry 2021-07-01
Series:Chemistry Journal of Moldova: General, Industrial and Ecological Chemistry
Subjects:
Online Access: http://www.cjm.asm.md/sites/default/files/article_files/ChemJMold_10.19261cjm.2021.820-Kulcitki.pdf
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spelling 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
work_keys_str_mv AT olgamorarescu onestepselectivesynthesisof13epimanoyloxide
AT marionelatraistari onestepselectivesynthesisof13epimanoyloxide
AT alicbarba onestepselectivesynthesisof13epimanoyloxide
AT gheorgheduca onestepselectivesynthesisof13epimanoyloxide
AT niconungur onestepselectivesynthesisof13epimanoyloxide
AT veaceslavkulcitki onestepselectivesynthesisof13epimanoyloxide
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