Similar articles for PMID: 31693792

Year	Number of Results
1984	1
1988	1
1995	1
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2005	1
2006	4
2009	3
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2012	7
2013	9
2014	5
2015	14
2016	10
2017	4
2018	2
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2020	12
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2024	1

1

Total Synthesis of (+)-6-epi-Ophiobolin A.

Thach DQ, Brill ZG, Grover HK, Esguerra KV, Thompson JK, Maimone TJ. Thach DQ, et al. Angew Chem Int Ed Engl. 2020 Jan 20;59(4):1532-1536. doi: 10.1002/anie.201913150. Epub 2019 Dec 12. Angew Chem Int Ed Engl. 2020. PMID: 31693792 Free PMC article.

2

Construction of the basic skeleton of ophiobolin A and variecolin.

Li K, Wang C, Yin G, Gao S. Li K, et al. Org Biomol Chem. 2013 Nov 21;11(43):7550-8. doi: 10.1039/c3ob41693c. Org Biomol Chem. 2013. PMID: 24096306

3

Ophiobolins P-T, five new cytotoxic and antibacterial sesterterpenes from the endolichenic fungus Ulocladium sp.

Wang QX, Bao L, Yang XL, Liu DL, Guo H, Dai HQ, Song FH, Zhang LX, Guo LD, Li SJ, Liu HW. Wang QX, et al. Fitoterapia. 2013 Oct;90:220-7. doi: 10.1016/j.fitote.2013.08.002. Epub 2013 Aug 13. Fitoterapia. 2013. PMID: 23954177

4

A general entry to antifeedant sesterterpenoids: total synthesis of (+)-norleucosceptroid A, (-)-norleucosceptroid B, and (-)-leucosceptroid K.

Hugelshofer CL, Magauer T. Hugelshofer CL, et al. Angew Chem Int Ed Engl. 2014 Oct 13;53(42):11351-5. doi: 10.1002/anie.201407788. Epub 2014 Sep 4. Angew Chem Int Ed Engl. 2014. PMID: 25196778

5

Preparation of cis-γ-hydroxycarvone derivatives for synthesis of sesterterpenoid natural products: total synthesis of phorbin A.

Hubert JG, Furkert DP, Brimble MA. Hubert JG, et al. J Org Chem. 2015 Feb 20;80(4):2231-9. doi: 10.1021/jo502748s. Epub 2015 Feb 5. J Org Chem. 2015. PMID: 25630043

6

Ophiobolin O and 6-epi-ophiobolin O, two new cytotoxic sesterterpenes from the marine derived fungus Aspergillus sp.

Zhang D, Fukuzawa S, Satake M, Li X, Kuranaga T, Niitsu A, Yoshizawa K, Tachibana K. Zhang D, et al. Nat Prod Commun. 2012 Nov;7(11):1411-4. Nat Prod Commun. 2012. PMID: 23285796

7

Enantioselective total synthesis of (+)-ophiobolin A.

Tsuna K, Noguchi N, Nakada M. Tsuna K, et al. Chemistry. 2013 Apr 22;19(17):5476-86. doi: 10.1002/chem.201204119. Epub 2013 Feb 28. Chemistry. 2013. PMID: 23447120

8

New Ophiobolin Derivatives from the Marine Fungus Aspergillus flocculosus and Their Cytotoxicities against Cancer Cells.

Choi BK, Trinh PTH, Lee HS, Choi BW, Kang JS, Ngoc NTD, Van TTT, Shin HJ. Choi BK, et al. Mar Drugs. 2019 Jun 11;17(6):346. doi: 10.3390/md17060346. Mar Drugs. 2019. PMID: 31212583 Free PMC article.

9

Ophiobolin E and 8-epi-ophiobolin J produced by Drechslera gigantea, a potential mycoherbicide of weedy grasses.

Evidente A, Andolfi A, Cimmino A, Vurro M, Fracchiolla M, Charudattan R, Motta A. Evidente A, et al. Phytochemistry. 2006 Oct;67(20):2281-7. doi: 10.1016/j.phytochem.2006.07.016. Epub 2006 Sep 7. Phytochemistry. 2006. PMID: 16962149

10

Chemistry and biology of ophiobolin A and its congeners.

Masi M, Dasari R, Evidente A, Mathieu V, Kornienko A. Masi M, et al. Bioorg Med Chem Lett. 2019 Apr 1;29(7):859-869. doi: 10.1016/j.bmcl.2019.02.007. Epub 2019 Feb 7. Bioorg Med Chem Lett. 2019. PMID: 30765189 Review.

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