Stereochemistry of enacyloxins 1. Absolute configuration of the cyclohexane ring part of enacyloxins, a series of antibiotics from Frateuria sp. W-315

DOI: 10.1515/HC.2001.7.4.327

Source and publish data:

Heterocyclic Communications p. 327 - 330 (2001)

Update date:2022-08-05

Topics:

Authors:

Fujimori, Toshitaka

Nakayama, Osamu

Kiyota, Hiromasa

Kamijima, Yu-Ichi

Watanabe, Toshihiko

Oritani, Takayuki

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Article abstract of DOI:10.1515/HC.2001.7.4.327

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

Full text of DOI:10.1515/HC.2001.7.4.327

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Article Doi

Stereochemistry of enacyloxins 1. Absolute configuration of the cyclohexane ring part of enacyloxins, a series of antibiotics from Frateuria sp. W-315

DOI: 10.1515/HC.2001.7.4.327

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Authors:

Article abstract of DOI:10.1515/HC.2001.7.4.327

Full text of DOI:10.1515/HC.2001.7.4.327

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