1977
DOI: 10.1016/0040-4020(77)80277-9
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Eudesmanolides derived from herbolide B

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1978
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Cited by 8 publications
(2 citation statements)
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“…Although, the NMR spectral data of 2 was very close with those of the previously synthesized compound (Sokoloff and Sfgal, 1977), compound 2 showed opposite optical rotation sign ½a 25 D ¼ þ4:16 (c = 0.048, CHCl 3 ), while the synthetic compound showed an ½a 25 D of À33 (c = 0.03, CHCl 3 ). Compound 2 was therefore the enantiomer of the reported synthetic compound and was identified as 1b,9b-diacetoxyeudesm-4-en-6b,11bH-12,6-olide, a new natural compound.…”
Section: Resultsmentioning
confidence: 53%
See 1 more Smart Citation
“…Although, the NMR spectral data of 2 was very close with those of the previously synthesized compound (Sokoloff and Sfgal, 1977), compound 2 showed opposite optical rotation sign ½a 25 D ¼ þ4:16 (c = 0.048, CHCl 3 ), while the synthetic compound showed an ½a 25 D of À33 (c = 0.03, CHCl 3 ). Compound 2 was therefore the enantiomer of the reported synthetic compound and was identified as 1b,9b-diacetoxyeudesm-4-en-6b,11bH-12,6-olide, a new natural compound.…”
Section: Resultsmentioning
confidence: 53%
“…Compound 1 was therefore, identified as 1b,9b-diacetoxyeudesm-3-en-5a,6b,11bH-12,6-olide and was a new natural compound and is reported here for the first time from a natural source (Sokoloff and Sfgal, 1977).…”
Section: Resultsmentioning
confidence: 97%