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

Heterocyclic Communications

Volumn 7, Issue 4, 2001, Pages 327-330

  Fujimori, Toshitaka ^a   Nakayama, Osamu ^a   Kiyota, Hiromasa ^a   Kamijima, Yu Ichi ^a   Watanabe, Toshihiko ^b   Oritani, Takayuki ^a  

^a TOHOKU UNIVERSITY   (Japan)

^b TOHOKU INSTITUTE OF TECHNOLOGY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0035730857     PISSN: 07930283     EISSN: None     Source Type: Journal    
DOI: 10.1515/HC.2001.7.4.327     Document Type: Article

References (16)

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13. 1H-NMR chemical shifts of both isomers: the H-1 peak of 12 was shifted lower field than that of (1R)-12 due to the deshielding effect of the O-3. This was also confirmed by converting 12 to 5. (matrix presented)
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16. 2 +32700).