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- The genus Micromonospora as a model microorganism for bioactive natural product discovery. Mohamed S. Hifnawy, Mohamed M. Fouda, Ahmed M. Sayed, Rabab Mohammed, Hossam M. Hassan, Sameh F. AbouZid, Mostafa E. Rateb, Alexander Keller, Martina Adamek, Nadine Ziemert, Usama Ramadan Abdelmohsen
, RSC Adv.
, 2020
, 10
, 20939
- Expansion of chemical space for natural products by uncommon P450 reactions. Xingwang Zhang, Shengying Li
, Nat. Prod. Rep.
, 2017
, 34
, 1061
- Index pages
, Nat. Prod. Rep.
, 1984
, 1
, I1
- Synthesis of 20-dihydro-20-deoxy derivatives of 16-membered macrolide antibiotics. Ashit K. Ganguly, Yi-Tsung Liu, Olga Sarre
, J. Chem. Soc., Chem. Commun.
, 1983
, 1166
- Samarium(ii) iodide-mediated reactions applied to natural product total synthesis. Majid. M. Heravi, Azadeh Nazari
, RSC Adv.
, 2022
, 12
, 9944
- Macrocyclic microbial metabolites. R. C. F. Jones
, Nat. Prod. Rep.
, 1984
, 1
, 87
- Mycinamicin biosynthesis: isolation and structural elucidation of mycinonic acids, proposed intermediates for formation of mycinamicins. X-Ray molecular structure of p-bromophenacyl 5-hydroxy-4-methylhept-2-enoate. Kenji Kinoshita, Satoshi Takenaka, Mitsuo Hayashi
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 2547
- The polyether and macrolide antibiotics: biogenetic analysis and structural correlations. D. O'Hagan
, Nat. Prod. Rep.
, 1989
, 6
, 205