Abstract
A synthesis of the proposed structure of cryptoconcatone H and one diastereoisomer has been achieved, featuring a tandem deprotection-oxa-Michael addition to establish the tetrahydropyran moiety. Comparison of the NMR spectroscopic data confirms that the original structural assignment was incorrect.
Original language | English |
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Article number | st-2018-d0654-l |
Pages (from-to) | 178-180 |
Number of pages | 3 |
Journal | Synlett |
Volume | 30 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2019 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© Georg Thieme Verlag Stuttgart New York.
ASJC Scopus Subject Areas
- Organic Chemistry
Keywords
- metathesis
- Michael addition
- stereochemistry
- tandem reaction
- tetrahydropyran