1956
DOI: 10.1021/ja01599a040
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The Chemistry of Fumagillin. IV. The Presence of an Epoxide Grouping and Other Observations on the Nature of the Oxygen Functions1

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Cited by 18 publications
(3 citation statements)
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“…Table I 1.8 " Irradiations were carried out on deoxygenated samples unless noted. 6 Irradiated both in the presence and absence of air, with the same results within experimental error.…”
Section: Sirsupporting
confidence: 59%
“…Table I 1.8 " Irradiations were carried out on deoxygenated samples unless noted. 6 Irradiated both in the presence and absence of air, with the same results within experimental error.…”
Section: Sirsupporting
confidence: 59%
“…Melting points were measured on a microscope hot plate and reported uncorrected. 6.68, 7.04 (2H each, d, J =8 Hz, -C 6 H4-0CHs in O-Me-Tyr). Cyl-2 was positive to 2,4-dinitrophenylhydrazine.…”
Section: Methodsmentioning
confidence: 99%
“…This compound previously had been prepared by Neber by esterification of o-aminophenylacetic acid. 6 The conversion into VIII was then carried out with benzoyl chloride in pyridine, in 72-78% yields based on nitroester, according to Neber's directions. 6 Ethyl o-Benzamidophenylacetate (IX).-Ethyl o-nitro-phenvlacetate14 was hydrogenated with platinum in absolute (9) J. N. Chatterjea, J. Indian Chem.…”
mentioning
confidence: 99%