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- Structure of ajugasterone C, a phytoecdysone with an 11-hydroxy-group. S. Imai, E. Murata, S. Fujioka, M. Koreeda, K. Nakanishi
, J. Chem. Soc. D
, 1969
, 546
- Interaction between non-adjacent benzoate groups: an extension of the dibenzoate chirality rule. M. Koreeda, N. Harada, K. Nakanishi
, J. Chem. Soc. D
, 1969
, 548
- Marine natural products from zoantharians: bioactivity, biosynthesis, systematics, and ecological roles. Paul O. Guillen, Karla B. Jaramillo, Grégory Genta-Jouve, Olivier P. Thomas
, Nat. Prod. Rep.
, 2020
, 37
, 515
- 14-Deoxymuristerone, a compound exhibiting exceptional moulting hormonal activity. Peter Cherbas, Diane A. Trainor, Richard J. Stonard, Koji Nakanishi
, J. Chem. Soc., Chem. Commun.
, 1982
, 1307
- Gerardiasterone, a new ecdysteroid with a 20,22,23,25-tetrahydroxylated side chain from the mediterranean zoanthid Gerardia savaglia. Antonio Guerriero, Pietro Traldi, Francesco Pietra
, J. Chem. Soc., Chem. Commun.
, 1986
, 40
- Taste and smell in aquatic and terrestrial environments. E. Mollo, M. J. Garson, G. Polese, P. Amodeo, M. T. Ghiselin
, Nat. Prod. Rep.
, 2017
, 34
, 496
- Secondary metabolites from marine sponges of the genus Agelas: a comprehensive update insight on structural diversity and bioactivity. Mei-Jun Chu, Meng Li, He Ma, Ping-Lin Li, Guo-Qiang Li
, RSC Adv.
, 2022
, 12
, 7789
- Subject index, 1969
, J. Chem. Soc. D
, 1969
, 1537
- Configurational and conformational studies of sugars by the aromatic chirality method. N. Harada, H. Sato, K. Nakanishi
, J. Chem. Soc. D
, 1970
, 1691
- Index pages
, Nat. Prod. Rep.
, 1986
, 3
, I1