Tetrahedron Letters 1963
DOI: 10.1016/b978-1-4831-9886-6.50018-8
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The Structure of Asperuloside

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Cited by 14 publications
(21 citation statements)
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“…In the course of studies on the constituents of the plants which are grown under a subtropical climate, we investigated the constituents of the leaves of Lasianthus wallichii (WIGHT & ARN.) Wight (Rubiaceae) and isolated two new compounds, one of which is bisiridoid glucoside (1) and the other non-glycosidic iridoid (2), together with five known compounds: asperuloside (3), 4) paederoside (4), 5,6) daphylloside (5), 7) citroside A (6), 8) benzyl 6-O-a -L-rhamnopyranosyl-b -D-glucopyranoside (7). 9) This paper deals with the isolation and structure elucidation of the new compounds.…”
mentioning
confidence: 99%
“…In the course of studies on the constituents of the plants which are grown under a subtropical climate, we investigated the constituents of the leaves of Lasianthus wallichii (WIGHT & ARN.) Wight (Rubiaceae) and isolated two new compounds, one of which is bisiridoid glucoside (1) and the other non-glycosidic iridoid (2), together with five known compounds: asperuloside (3), 4) paederoside (4), 5,6) daphylloside (5), 7) citroside A (6), 8) benzyl 6-O-a -L-rhamnopyranosyl-b -D-glucopyranoside (7). 9) This paper deals with the isolation and structure elucidation of the new compounds.…”
mentioning
confidence: 99%
“…spectra (A,,, 204 nm) indicated the presence of an en01 ether function (2). 1 gave black polymers on acid treatment, a property which has been shown to be characteristic of most iridoid compounds (3,4). The latter designation gained further support by the presence of a one-proton signal at 6.13 p.p.m.…”
Section: La ~Nentzeloside (I) Rel-(i R4nr5r6r7s7ar) Epoxy-67-0mentioning
confidence: 76%
“…Occidentoside (III) and its monomethyl ether (VIII), on acetylation, furnished a hexaacetate (IX) and a pentaacetate (X) respectively. The PMR spectra (CDC13) of these two acetates showed very close resemblance and revealed in both, the presence of six and five acetoxyl groups (7.72-8.00) respectively and C1-C6 protons of the glucose moiety as large multiplets [28] between 4.62 and 6.20. The presence of the two low field protons could be inferred in each acetate as in the two methyl ethers by the bathochro-OH2 L :0 mic shifts on addition of A1C13 to the test solution, (1) hexaacetate: (a) 281 -316 nm (A-5), (b) 366-* 419 nm (D-6"), (2) pentaacetate: (a) 284-321 nm (A- 5), (b) 375 -430 nm (D-6").…”
Section: Resultsmentioning
confidence: 93%