Structural basis of the Cope rearrangement and cyclization in hapalindole biogenesis-Reference-Cited by-同舟云学术

Structural basis of the Cope rearrangement and cyclization in hapalindole biogenesis

Published:2018-03-12 Issue:4 Volume:14 Page:345-351
ISSN:1552-4450
Container-title:Nature Chemical Biology
language:en
Short-container-title:Nat Chem Biol

Author:

Newmister Sean A.,Li Shasha,Garcia-Borràs Marc^ORCID,Sanders Jacob N.,Yang Song,Lowell Andrew N.,Yu Fengan,Smith Janet L.,Williams Robert M.,Houk K. N.,Sherman David H.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology

Link

http://www.nature.com/articles/s41589-018-0003-x.pdf

Reference54 articles.

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2. Asthana, R. K. et al. Identification of an antimicrobial entity from the cyanobacterium Fischerella sp. isolated from bark of Azadirachta indica (Neem) tree. J. Appl. Phycol. 18, 33–39 (2006).

3. Becher, P. G., Keller, S., Jung, G., Süssmuth, R. D. & Jüttner, F. Insecticidal activity of 12-epi-hapalindole J isonitrile. Phytochemistry 68, 2493–2497 (2007).

4. Cagide, E. et al. Hapalindoles from the cyanobacterium Fischerella: potential sodium channel modulators. Chem. Res. Toxicol. 27, 1696–1706 (2014).

5. Mo, S., Krunic, A., Chlipala, G. & Orjala, J. Antimicrobial ambiguine isonitriles from the cyanobacterium Fischerella ambigua. J. Nat. Prod. 72, 894–899 (2009).

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