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Journal article

Total synthesis of the Schisandraceae nortriterpenoid rubriflordilactone A

Abstract:
Full details of the total synthesis of the Schisandraceae nortriterpenoid natural product rubriflordilactone A are reported. Palladium- and cobalt-catalyzed polycyclizations were employed as key strategies to construct the central pentasubstituted arene from bromoendiyne and triyne precursors. This required the independent assembly of two AB ring aldehydes for combination with a common diyne component. A number of model systems were explored to investigate these two methodologies, and also to establish routes for the installation of the challenging benzopyran and butenolide rings.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1002/chem.201703229

Authors


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Institution:
University of Oxford
Oxford college:
Jesus College
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author


More from this funder
Grant:
additionalfunding(EP/K005391/1
AdvancedResearchFellowship (EAA)(EP/E055273/1)
More from this funder
Grant:
Marie Skłodowska-Curie actions for an Individual Fellowship (GC, GA N° 656012


Publisher:
Wiley
Journal:
Chemistry More from this journal
Volume:
23
Issue:
56
Pages:
14080–14089
Publication date:
2017-09-08
Acceptance date:
2017-08-01
DOI:
ISSN:
1521-3765


Language:
English
Keywords:
Pubs id:
pubs:713283
UUID:
uuid:f33ab4c4-22b3-4443-9efe-5d038e884be4
Local pid:
pubs:713283
Source identifiers:
713283
Deposit date:
2017-08-11

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