Journal article
Recent applications in natural product synthesis of dihydro-furan and -pyran formation by ring-closing alkene metathesis
- Abstract:
- In the last two decades, alkene metathesis has risen in prominence to become a significant synthetic strategy for alkene formation. Many total syntheses of natural products have used this transformation. We review the use, from 2003 to 2015, of ring-closing alkene metathesis (RCM) for the generation of dihydro-furans or -pyrans in natural product synthesis. The strategies used to assemble the RCM precursors and the subsequent use of the newly formed unsaturation will also be highlighted and placed in context.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 4.3MB, Terms of use)
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- Publisher copy:
- 10.1039/C6OB00593D
Authors
+ Engineering and Physical Sciences Research Council
More from this funder
- Funding agency for:
- Jacques, R
- Pal, R
- Parker, N
- Sear, C
- Smith, P
- Grant:
- EP/L015838/1
- EP/L015838/1
- EP/L015838/1
- EP/L015838/1
- EP/L015838/1
- Publisher:
- Royal Society of Chemistry
- Journal:
- Organic and Biomolecular Chemistry More from this journal
- Volume:
- 14
- Issue:
- 25
- Pages:
- 5875-5893
- Publication date:
- 2016-04-25
- Acceptance date:
- 2016-04-13
- DOI:
- EISSN:
-
1477-0539
- ISSN:
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1477-0520
- Pubs id:
-
pubs:615173
- UUID:
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uuid:c9ba6bd1-2be1-4ff0-8b8a-800d8e8b640d
- Local pid:
-
pubs:615173
- Source identifiers:
-
615173
- Deposit date:
-
2016-04-13
- ARK identifier:
Terms of use
- Copyright holder:
- Jacques et al
- Copyright date:
- 2016
- Notes:
- This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
- Licence:
- CC Attribution (CC BY)
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