Heterocyclic Communications p. 327 - 330 (2001)
Update date:2022-08-05
Topics:
Fujimori, Toshitaka
Nakayama, Osamu
Kiyota, Hiromasa
Kamijima, Yu-Ichi
Watanabe, Toshihiko
Oritani, Takayuki
The stereochemical study of the cyclohexane ring part of enacyloxins (ENXs), a series of antibiotics isolated from Frateuria sp. W-315, was examined. The relative configuration was elucidated by the coupling constant values of the 1H NMR spectr
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