Eugenunilones A–H: rearranged sesquiterpenoids from Eugenia uniflora. Issue 3 (16th December 2021)
- Record Type:
- Journal Article
- Title:
- Eugenunilones A–H: rearranged sesquiterpenoids from Eugenia uniflora. Issue 3 (16th December 2021)
- Main Title:
- Eugenunilones A–H: rearranged sesquiterpenoids from Eugenia uniflora
- Authors:
- Chen, Mu
Cao, Jia-Qing
Ang, Song
Zeng, Ting-Ni
Li, Ni-Ping
Yang, Tang-Jia
Liu, Jun-Shan
Wu, Yan
Ye, Wen-Cai
Wang, Lei - Abstract:
- Abstract : Six rearranged sesquiterpenoids (1–6 ) with four types of new polycyclic caged skeletons were isolated from Eugenia uniflora . Abstract : Six rearranged sesquiterpenoid dimers and monomers with four types of new skeletons, meso -eugenunilone A ( meso -1 ), (+)- and (−)-eugenunilones B−F [(+)- and (−)-2 –6 ], along with two new biogenetically related members (+)- and (−)-eugenunilones G−H [(+)- and (−)-7 and 8 ] and a known one (9 ), were isolated from the fruits of Eugenia uniflora . Compounds 1 and 2 were two unprecedented dimers with caged tricyclo[4.4.0.0 2, 8 ]decane units. Compounds 3 and 4 represent the first examples of sesquiterpenoids possessing a caged tricyclo[4.3.1.0 3, 7 ]decane core and an isopentyl substituted bicyclo[3.2.1]octane backbone, respectively, while compounds 5 and 6 share a tricyclo[4.4.0.0 2, 10 ]decane scaffold which is found in nature for the first time. In particular, compounds 2–9 were successfully separated into eight pairs of optically pure enantiomers by chiral HPLC separation. Their structures and absolute configurations were unambiguously established by a combination of spectroscopic data, X-ray diffraction analysis, and electronic circular dichroism (ECD) calculations. A hypothetical biogenetic pathway for these new compounds was proposed. It is interesting that these diverse frameworks were all derived from the same bicyclic precursor (9 ). In addition, compounds 2, 4, and 6 showed moderate anti-inflammatory effects inAbstract : Six rearranged sesquiterpenoids (1–6 ) with four types of new polycyclic caged skeletons were isolated from Eugenia uniflora . Abstract : Six rearranged sesquiterpenoid dimers and monomers with four types of new skeletons, meso -eugenunilone A ( meso -1 ), (+)- and (−)-eugenunilones B−F [(+)- and (−)-2 –6 ], along with two new biogenetically related members (+)- and (−)-eugenunilones G−H [(+)- and (−)-7 and 8 ] and a known one (9 ), were isolated from the fruits of Eugenia uniflora . Compounds 1 and 2 were two unprecedented dimers with caged tricyclo[4.4.0.0 2, 8 ]decane units. Compounds 3 and 4 represent the first examples of sesquiterpenoids possessing a caged tricyclo[4.3.1.0 3, 7 ]decane core and an isopentyl substituted bicyclo[3.2.1]octane backbone, respectively, while compounds 5 and 6 share a tricyclo[4.4.0.0 2, 10 ]decane scaffold which is found in nature for the first time. In particular, compounds 2–9 were successfully separated into eight pairs of optically pure enantiomers by chiral HPLC separation. Their structures and absolute configurations were unambiguously established by a combination of spectroscopic data, X-ray diffraction analysis, and electronic circular dichroism (ECD) calculations. A hypothetical biogenetic pathway for these new compounds was proposed. It is interesting that these diverse frameworks were all derived from the same bicyclic precursor (9 ). In addition, compounds 2, 4, and 6 showed moderate anti-inflammatory effects in zebrafish acute inflammatory models. … (more)
- Is Part Of:
- Organic chemistry frontiers. Volume 9:Issue 3(2022)
- Journal:
- Organic chemistry frontiers
- Issue:
- Volume 9:Issue 3(2022)
- Issue Display:
- Volume 9, Issue 3 (2022)
- Year:
- 2022
- Volume:
- 9
- Issue:
- 3
- Issue Sort Value:
- 2022-0009-0003-0000
- Page Start:
- 667
- Page End:
- 675
- Publication Date:
- 2021-12-16
- Subjects:
- Chemistry, Organic -- Periodicals
547.005 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/qo#!recentarticles&all ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1qo01629f ↗
- Languages:
- English
- ISSNs:
- 2052-4110
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6287.121000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21114.xml