2001
DOI: 10.1271/bbb.65.810
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Identification of 2,3-Dihydro-γ-ionylideneethanol in Cercospora cruenta

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Cited by 6 publications
(6 citation statements)
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“…However, as most of the micro‐organisms are phytopathogens (Yamamoto et al . ; Siewers et al . ), the practical application of micro‐organisms to grapevine to promote anthocyanin biosynthesis in grape berry skin has not been reported.…”
Section: Grape Skin Colour Alteration By Micro‐organismsmentioning
confidence: 99%
“…However, as most of the micro‐organisms are phytopathogens (Yamamoto et al . ; Siewers et al . ), the practical application of micro‐organisms to grapevine to promote anthocyanin biosynthesis in grape berry skin has not been reported.…”
Section: Grape Skin Colour Alteration By Micro‐organismsmentioning
confidence: 99%
“…C. rosicola converted FDP to ABA (Bennett et al, 1984), and C. rosicola and C. cruenta metabolized 2Z,4E-a-ionylideneethanol (6) and 2Z,4E-c-ionylideneethanol (7), respectively, to ABA (Neill et al, 1987;Oritani et al, 1985;Kato et al, 1987). However, putative intermediates between FDP and ionylideneethanol, 4,5-didehydrofarnesol and monocyclofarnesol, were not converted to ABA, and their production by these fungi has not been confirmed (Bennett et al, 1990;Yamamoto and Oritani, 1997;Yamamoto et al, 2001). This is a shortcoming in support of the direct pathway.…”
Section: Introductionmentioning
confidence: 99%
“…Their structure elucidation was conducted as following described and H‐atom and carbon NMR values assigned ( Table ). Compound 2 was identified as (–)‐ cis ‐ γ ‐monocyclofarnesol, which, to the best of our knowledge, has never been isolated to date from natural sources whereas it was described as synthesis product . In particular, the racemic mixture (±)‐ 2 and the (+)‐ 2 enantiomer were synthesized several years ago and partially characterized.…”
Section: Resultsmentioning
confidence: 99%
“…Compound 2 was identified as (-)cis-c-monocyclofarnesol, which, to the best of our knowledge, has never been isolated to date from natural sources whereas it was described as synthesis product. [28 -30] In particular, the racemic mixture (AE)-2 [28] [29] and the (+)-2 enantiomer [30] were synthesized several years ago and partially characterized. Due to this, fully NMR assignment of compound 2 has been also reported here ( Table 1).…”
Section: Resultsmentioning
confidence: 99%