## Abstract Carbonβ13 NMR signals of the biologically active norditerpenoid dilactones from __Podocarpus__ plants were fully assigned by using selective ^1^H decoupling, coupling constants (^2^__J__~CH~), spinβlattice relaxation times (__T__~1~) and correlation of the spectra of more than thirty di
β¦ LIBER β¦
Total synthesis of nagilactone F, biologically active nor-diterpenoid dilactone isolated from podocarpus nagi
β Scribed by Yuji Hayashi; Takeshi Matsumoto; Toshiaki Hyono; Naomi Nishikawa; Motokazu Uemura; Mugio Nishizawa; Masatoshi Togami; Takeo Sakan
- Book ID
- 104246391
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- French
- Weight
- 267 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Nagilactone F was synthesized from (+)-podocarpic acid of the established structure. This work constitutes the first total synthesis of the biologically active norditerpenoid dilactones in Podocarpus plants.
Nor-and bisnor-diterpenoid dilactones 2a) , isolated from various species of Podocarpus plants, constitute an important group of compounds in natural product chemistry, since a wide variety of their biological activities 3) , as well as
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