A Convergent and Stereocontrolled Cycloaddition Strategy toward Eudesmane Sesquiterpenoid: Total Synthesis of (±)-6β,14-Epoxyeudesm-4(15)-en-1β-ol-Reference-Cited by-同舟云学术

A Convergent and Stereocontrolled Cycloaddition Strategy toward Eudesmane Sesquiterpenoid: Total Synthesis of (±)-6β,14-Epoxyeudesm-4(15)-en-1β-ol

Published:2012-04-18 Issue:9 Volume:77 Page:4217-4225
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wang Cui-Cui¹,Li Wei-Dong Z.¹²

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China

2. State Key Laboratory of Elemento-organic Chemistry, Nankai University, Tianjin 300071, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo300556r

Reference42 articles.

1. aHeathcock, C. H.InThe Total Synthesis of Natural Products;ApSimon, J., Ed.John Wiley and Sons:New York, 1973; Vol.2, pp197–558.

2. Celastraceae sesquiterpenoids: biological activity and synthesis

3. Eudesmane sesquiterpenoids from the Asteraceae family

4. aMunoz, O.; Penazola, A.; Gonzales, A. G.; Ravelo, A. G.; Bazzocchi, I. L.; Alvarenga, N. L.InStudies in Natural Product Chemistry;Atta-ür-Rahman, Ed.Elsevier Science Publisher:Amsterdam, 1996; Vol.18, pp739–783.

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