Tandem C–H oxidation/cyclization/rearrangement and its application to asymmetric syntheses of (−)-brussonol and (−)-przewalskine E-Reference-Cited by-同舟云学术

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Tandem C–H oxidation/cyclization/rearrangement and its application to asymmetric syntheses of (−)-brussonol and (−)-przewalskine E

Published:2015-06-17 Issue:1 Volume:6 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Jiao Zhi-Wei,Tu Yong-Qiang,Zhang Qing,Liu Wen-Xing,Zhang Shu-Yu,Wang Shao-Hua,Zhang Fu-Min,Jiang Sen

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms8332.pdf

Reference58 articles.

1. Xu, G. et al. Przewalskone: a cytotoxic adduct of a danshenol type terpenoid and an icetexane diterpenoid via hetero-Diels–Alder reaction from Salvia przewalskii. Chem. Commun. 48, 4438–4440 (2012).

2. Aoyagi, Y. et al. Semisynthesis of isetexane diterpenoid analogues and their cytotoxic activity. Chem. Pharm. Bull. 54, 1602–1604 (2006).

3. McGrath, N. A., Bartlett, E. S., Sittihan, S. & Njardarson, J. T. A concise ring-expansion route to the compact core of platensimycin. Angew. Chem. Int. Ed. 48, 8543–8546 (2009).

4. Marson, C. M., Campbell, J., Hursthouse, M. B. & Abdul Malik, K. M. Stereocontrolled routes to bridged ethers by tandem cyclizations. Angew. Chem. Int. Ed. 37, 1122–1124 (1998).

5. Wu, Y., Li, Y. & Wu, Y.-L. First examples of Friedel–Crafts alkylation using ketals as alkylating agents: an expeditious access to the benzene-fused 8-oxabicyclo[3.2.1]octane ring system. J. Chem. Soc. Perkin Trans. 1 1189–1192 (1999).

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