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Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance spectroscopy

https://doi.org/10.1021/ja00479a014
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Glycosyl Imidates, 56. Synthesis of the Hexasaccharide Moiety of Pectinioside E
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The Structure of Verbascosaponin
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Studies on the Constituents of the Stems of Tinospora tuberculata, IV. Isolation and Structure Elucidation of the Five New Furanoid Diterpene Glycosides Borapetoside C–G
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The structure of hellebrin
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Spirostanol glycoside from the tuber of Ophiopogon japonicus
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1H and 13C NMR spectra of derivatives of 2‐hydroxy‐3‐methylbut‐3‐enenitrile and 2‐hydroxy‐3‐methylbut‐2‐enenitrile
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Differentiation of diastereomeric 2‐substituted cyclohexanamines with three chirality centres by 13C NMR spectroscopy
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Stereochemical factors determining the effects of glycosylation on the 13C chemical shifts in carbohydrates
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Carbon‐13 NMR studies of monohydroxylated and monochlorinated derivatives of Z‐ and E‐p‐menthanes
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Glucosidation shifts of allylic and benzylic alcohols in 13C NMR spectroscopy
inferred← citeshttps://doi.org/10.1002/ptr.2894openalex-snapshot
Antiplasmodial activities of furoquinoline alkaloids from Teclea afzelii
inferred← citeshttps://doi.org/10.1007/978-1-4612-3006-9_2openalex-snapshot
Carbon-13 NMR Spectroscopy of Steroidal Alkaloids
inferred← citeshttps://doi.org/10.1007/978-1-4613-0413-5_19openalex-snapshot
A Novel Triterpenoid Saponin from the Leaves of Majorana Hortensis (MOENCH)
inferred← citeshttps://doi.org/10.1007/978-1-4613-0413-5_22openalex-snapshot
Steroidal Glycosides from Nicotiana Tabacum L. Seeds and their Biological Activity
inferred← citeshttps://doi.org/10.1007/978-1-4613-0413-5_3openalex-snapshot
Intensely Sweet Saponin Osladin: Synthetic and Structural Study
inferred← citeshttps://doi.org/10.1007/978-1-4899-1367-8_34openalex-snapshot
Phyto-Pharmacology of Saponins from Symphytum officinale L.
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Triterpene Glycosides from Sophora japonica L. Seeds
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Steroidal Saponins
inferred← citeshttps://doi.org/10.1007/bf00567289openalex-snapshot
13C NMR spectra of acetylated hederagenin glycosides
inferred← citeshttps://doi.org/10.1007/bf00575046openalex-snapshot
13C NMR spectra of steroid glycosides. II. Acetates of pennogenin glycosides
inferred← citeshttps://doi.org/10.1007/bf00575700openalex-snapshot
13C NMR spectra of steroid glycosides. III. Acetates of pennogenin triosides
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Triterpene saponins fromThalictrum minus. V. Structure of thalicoside B
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Triterpene saponins fromThalictrum minus. IV. The structure of thalicoside A
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13C NMR spectra of steroid clycosides. I. Pennogenin glycosides
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Triterpene glycosides of Thalictrum squarrosum. IV. Structures of squarrosides A1, A2, B1, and B2
inferred← citeshttps://doi.org/10.1007/bf00598578openalex-snapshot
Triterpene glycosides of Hedera taurica
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Structure of the main flavonoid glycoside from the flowers ofFilipendula ulmaria
inferred← citeshttps://doi.org/10.1007/bf00600827openalex-snapshot
Triterpene glycosides ofHedera taurica I. Structure of tauroside E from the leaves ofHedera taurica
inferred← citeshttps://doi.org/10.1007/bf00602458openalex-snapshot
Structure of the coumarin glycoside reoselin from the roots ofFerula kirialovii
inferred← citeshttps://doi.org/10.1007/bf00629974openalex-snapshot
Triterpene saponins fromThalictrum minus. VIII. Structure of thalicoside D
inferred← citeshttps://doi.org/10.1007/bf00630077openalex-snapshot
Triterpene glycosides of Hedera taurica VI. Structures of hederosides G, H1, H2, and I from the berries of Crimean ivy
inferred← citeshttps://doi.org/10.1007/bf00630172openalex-snapshot
Steroids of the spirostan and furostan series from Nolina microcarpa IV. Structures of nolinogenin, nolinospiroside B, and nolinofuroside B
inferred← citeshttps://doi.org/10.1007/bf00630361openalex-snapshot
Steroids of the spirostan and furostan series from Nolina microcarpa I. Structures of nolinospiroside C and nolinofurosides A and C
inferred← citeshttps://doi.org/10.1007/bf00630363openalex-snapshot
Triterpene glycosides of Hedera taurica VII. Structures of taurosides A and D from the leaves of Crimean ivy
inferred← citeshttps://doi.org/10.1007/bf00630577openalex-snapshot
Triterpene saponins fromThalictrum minus. VII. Structure of thalicoside E
inferred← citeshttps://doi.org/10.1007/bf00630603openalex-snapshot
Steroid glycosides ofNicotiana tabacum seeds I. The structures of nicotianosides A, B, and E
inferred← citeshttps://doi.org/10.1007/bf00630649openalex-snapshot
Triterpene glycosides of Hedera taurica
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Triterpene saponins from Thalictrum minus. VI. Structure of thalicoside C
inferred← citeshttps://doi.org/10.1007/bf00633392openalex-snapshot
Triterpene glycosides of Hedera taurica. III. Structures of hederosides A3, B, E2 and F from the berries of Crimean ivy
inferred← citeshttps://doi.org/10.1007/bf01164887openalex-snapshot
Triterpene glycosides ofSophora japonica seeds
inferred← citeshttps://doi.org/10.1007/bf01165196openalex-snapshot
Steroid glycosides of the seeds ofNicotiana tabacum. II. The structures of nicotianosides C and F
inferred← citeshttps://doi.org/10.1007/bf01434236openalex-snapshot
New triterpene glycosides fromThalictrum squarrosum St. ex Willd. The structure of squarrosides B3 and B4
inferred← citeshttps://doi.org/10.1007/bf01870610openalex-snapshot
Solasodine glycosides of Solanum unguiculatum (A.) Rich
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Platyphylloside: Metabolism and digestibility reductionin vitro
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New triterpenoid glycosides fromThalictrum minus L.
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New triterpenoid glycosides fromThalictrum minus L.
inferred← citeshttps://doi.org/10.1007/bf02499086openalex-snapshot
Structural characterization of gentiobiosyl diglycerides fromBacillus pumilus associated with ascidiaHalocynthia aurantium
inferred← citeshttps://doi.org/10.1007/bf02709296openalex-snapshot
Β-Sitosterol-3-O-β-D-xylopyranoside from the flowers ofTridax procumbens Linn
inferred← citeshttps://doi.org/10.1007/bf02856301openalex-snapshot
Carbon-13 NMR spectra of phytolaccagenin and its glycosides
inferred← citeshttps://doi.org/10.1007/bf02857779openalex-snapshot
New triterpenoid saponins fromIlex pubescens
inferred← citeshttps://doi.org/10.1007/bf02872573openalex-snapshot
Novel triterpenoidal saponin from the seeds ofPithecellobium dulce
inferred← citeshttps://doi.org/10.1007/bf02972979openalex-snapshot
Iridoid glycosides isolated fromOldenlandia diffusa inhibit LDL-oxidation
inferred← citeshttps://doi.org/10.1007/bf02973986openalex-snapshot
Triterpenoid saponins from the roots ofCaragana sinica
inferred← citeshttps://doi.org/10.1007/s10600-005-0096-9openalex-snapshot
Structural Studies and Biological Activity of Plant Triterpenoids from the Thalictrum Genus
inferred← citeshttps://doi.org/10.1007/s10600-009-9408-9openalex-snapshot
Antibacterial activity of the chemical constituents from Ranunculus laetus
inferred← citeshttps://doi.org/10.1007/s10600-012-0244-yopenalex-snapshot
Antiplasmodial activity of compounds from Drypetes gerrardii
inferred← citeshttps://doi.org/10.1007/s10600-014-0825-zopenalex-snapshot
A Steroidal Saponin from the Seeds of Allium tuberosum
inferred← citeshttps://doi.org/10.1007/s10600-020-03219-4openalex-snapshot
A New Flavone C-Glucoside from Aquilaria agallocha
inferred← citeshttps://doi.org/10.1007/s10600-024-04348-wopenalex-snapshot
Chemical Constituents of the Flowers of Aquilaria agallocha
inferred← citeshttps://doi.org/10.1007/s10600-024-04466-5openalex-snapshot
A New Minor Hederagenin-Type Triterpene Saponin from Cassia fistula
inferred← citeshttps://doi.org/10.1007/s10600-024-04476-3openalex-snapshot
Secondary Metabolites of Mangifera indica
inferred← citeshttps://doi.org/10.1007/s10600-025-04839-4openalex-snapshot
Diarylheptanoids from Alnus incana
inferred← citeshttps://doi.org/10.1007/s10787-017-0310-yopenalex-snapshot
RETRACTED ARTICLE: Novel glycoside from Wedelia calendulacea inhibits diethyl nitrosamine-induced renal cancer via downregulating the COX-2 and PEG2 through nuclear factor-κB pathway
inferred← citeshttps://doi.org/10.1007/s11418-010-0436-3openalex-snapshot
Three new aromatic glycosides from the ripe fruit of cherry tomato
inferred← citeshttps://doi.org/10.1007/s11418-010-0464-zopenalex-snapshot
Components of convolvulin from Quamoclit × multifida
inferred← citeshttps://doi.org/10.1007/s11418-012-0730-3openalex-snapshot
Two new glycosidic acids, multifidinic acids F and G, of the ether-insoluble resin glycoside (convolvulin) from the seeds of Quamoclit × multifida
inferred← citeshttps://doi.org/10.1007/s11418-019-01366-9openalex-snapshot
Identification and characterization of organic and glycosidic acids in crude resin glycoside fraction from Calystegia hederacea
inferred← citeshttps://doi.org/10.1007/s11418-022-01669-4openalex-snapshot
Identification and characterization of organic and glycosidic acids in the crude resin glycoside fraction from the leaves and stems of Calystegia japonica
inferred← citeshttps://doi.org/10.1007/s11418-023-01720-yopenalex-snapshot
Five new resin glycosides, calyhedins XI–XV, from Calystegia hederacea
inferred← citeshttps://doi.org/10.1007/s11418-024-01838-7openalex-snapshot
Eleven new glycosidic acid methyl esters from the crude resin glycoside fraction of Ipomoea alba seeds
inferred← citeshttps://doi.org/10.1007/s11418-024-01868-1openalex-snapshot
Ten new resin glycosides, ipoalbins I–X, from Ipomoea alba seeds
inferred← citeshttps://doi.org/10.1007/s11418-025-01877-8openalex-snapshot
Four new acylated glycosidic acid methyl esters and a new glycosidic acid from Ipomoea lacunosa seeds
inferred← citeshttps://doi.org/10.1007/s12010-014-0889-zopenalex-snapshot
Biosynthesis of Glucosyl Glycerol, a Compatible Solute, Using Intermolecular Transglycosylation Activity of Amylosucrase from Methylobacillus flagellatus KT
inferred← citeshttps://doi.org/10.1016/0008-6215(83)88269-xopenalex-snapshot
Structural studies of the O-specific polysaccharide from Serratia marcescens N.C.T.C. 1377
inferred← citeshttps://doi.org/10.1016/0008-6215(84)85196-4openalex-snapshot
Dependence of 13C chemical shifts on the spatial interaction of protons, and its application in structural and conformational studies of oligo- and poly-saccharides
inferred← citeshttps://doi.org/10.1016/0008-6215(85)85014-xopenalex-snapshot
Methods for the preparation of alkyl 1,2-orthoacetates of d-glucopyranose and d-galactopyranose in high yield
inferred← citeshttps://doi.org/10.1016/0008-6215(90)80004-mopenalex-snapshot
Synthesis and n.m.r. spectral properties of grape monoterpenyl glycosides
inferred← citeshttps://doi.org/10.1016/0008-6215(90)84292-3openalex-snapshot
Solution behavior of methyl β-xylobioside: Conformational flexibility revealed by n.m.r. measurements and theoretical calculations
inferred← citeshttps://doi.org/10.1016/0008-6215(91)80144-copenalex-snapshot
A nuclear magnetic resonance spectroscopic and conformational study of eight pseudo-trehaloses (d-glucopyranosyl 5a-carba-d- and -l-glucopyranosides)
inferred← citeshttps://doi.org/10.1016/0008-6215(96)00011-0openalex-snapshot
Synthesis of O- and S-glucosides using glucosyl halides and zinc salts
inferred← citeshttps://doi.org/10.1016/0031-9422(80)80203-2openalex-snapshot
Grayanoside C, a new diterpene glucoside from Leucothoe grayana
inferred← citeshttps://doi.org/10.1016/0031-9422(80)83026-3openalex-snapshot
Steroidal alkaloids from Solanum khasian um: Application of 13C NMR spectroscopy to their structural elucidation
inferred← citeshttps://doi.org/10.1016/0031-9422(82)80022-8openalex-snapshot
Acalyphin, a cyanogenic glucoside from Acalypha indica
inferred← citeshttps://doi.org/10.1016/0031-9422(82)80023-xopenalex-snapshot
Sarmentosin epoxide, a new cyanogenic compound from Sedum cepaea
inferred← citeshttps://doi.org/10.1016/0031-9422(82)80029-0openalex-snapshot
Iridoid glycosides of Rehmannia glutinosa
inferred← citeshttps://doi.org/10.1016/0031-9422(83)80162-9openalex-snapshot
6β-Hydroxyursolic acid and other triterpenoids of Enkianthus cernuus
inferred← citeshttps://doi.org/10.1016/0031-9422(84)83039-3openalex-snapshot
Two saponins from Zexmenia buphthalmiflora
inferred← citeshttps://doi.org/10.1016/0031-9422(86)80025-5openalex-snapshot
Structure of linifolioside, an isopimarane rhamnoglucoside from Leucas linifolia
inferred← citeshttps://doi.org/10.1016/0031-9422(88)80001-3openalex-snapshot
Triterpenoid saponins
inferred← citeshttps://doi.org/10.1016/0031-9422(88)80016-5openalex-snapshot
Digitoxigenin-3β-O-[β-d-fucopyranosyl-4′-β-d-glucopyranoside], the main cardenolide of somatic embryos of Digitalis lanata
inferred← citeshttps://doi.org/10.1016/0031-9422(88)80029-3openalex-snapshot
Pentacyclic triterpenoid rhamnosides from Combretum imberbe leaves
inferred← citeshttps://doi.org/10.1016/0031-9422(88)80033-5openalex-snapshot
The steroidal glycosides of the flowers of Yucca gloriosa
inferred← citeshttps://doi.org/10.1016/0031-9422(88)80057-8openalex-snapshot
Spirostanol glycoside from fruits of Asparagus officinalis
inferred← citeshttps://doi.org/10.1016/0031-9422(88)80211-5openalex-snapshot
New triterpenoid saponins from Corchorus acutangulus
inferred← citeshttps://doi.org/10.1016/0031-9422(88)80223-1openalex-snapshot
Acylated flavonols from Crocosmia crocosmiiflora
inferred← citeshttps://doi.org/10.1016/0031-9422(88)80310-8openalex-snapshot
A soyasapogenol-B glucoside from the seeds of Phaseolus vulgaris
inferred← citeshttps://doi.org/10.1016/0031-9422(88)80692-7openalex-snapshot
Atratosides A, B, C and D, steroid glycosides from the root of Cynanchum atratum
inferred← citeshttps://doi.org/10.1016/0031-9422(89)80054-8openalex-snapshot
Triterpenoid saponins from Randia uliginosa fruits
inferred← citeshttps://doi.org/10.1016/0031-9422(89)80152-9openalex-snapshot
Ergosta-7,22-dien-3β-ol glycoside from Tylopilus neofelleus
inferred← citeshttps://doi.org/10.1016/0031-9422(89)85039-3openalex-snapshot
Structure of acaciaside, a triterpenoid trisaccharide from Acacia auriculiformis
inferred← citeshttps://doi.org/10.1016/0031-9422(90)80151-6openalex-snapshot
Terpenoid glycosides from Ophiopogon japonicus roots
inferred← citeshttps://doi.org/10.1016/0031-9422(90)83073-aopenalex-snapshot
Sterol glucosides from Prunella vulgaris
inferred← citeshttps://doi.org/10.1016/0031-9422(90)85044-gopenalex-snapshot
Astrailienin a from Astragalus iliensis
inferred← citeshttps://doi.org/10.1016/0031-9422(90)85065-nopenalex-snapshot
Saponins from Oxytropis glabra
inferred← citeshttps://doi.org/10.1016/0031-9422(90)85184-hopenalex-snapshot
Caffeine and theanine from cultured cells of Camellia sinensis
inferred← citeshttps://doi.org/10.1016/0031-9422(90)85229-9openalex-snapshot
A triterpene saponin from Cylicodiscus gabunensis
inferred← citeshttps://doi.org/10.1016/0031-9422(90)85277-mopenalex-snapshot
Scammonins I and II, the resin glycosides of radix scammoniae from Convolvulus scammonia
inferred← citeshttps://doi.org/10.1016/0031-9422(90)85356-kopenalex-snapshot
Anthraquinones from Rhamnus formosana
inferred← citeshttps://doi.org/10.1016/0031-9422(90)89040-gopenalex-snapshot
Pregnane glycosides from Boucerosia aucheriana
inferred← citeshttps://doi.org/10.1016/0031-9422(90)89070-popenalex-snapshot
Spirostanol saponins from Yucca aloifolia rhizomes
inferred← citeshttps://doi.org/10.1016/0031-9422(91)80035-yopenalex-snapshot
Triterpenoid glycosides from Stauntonia hexaphylla
inferred← citeshttps://doi.org/10.1016/0031-9422(91)83043-kopenalex-snapshot
Glycosides of a cycloartane sapogenin fromCurculigo orchioides
inferred← citeshttps://doi.org/10.1016/0031-9422(91)83215-7openalex-snapshot
Triterpenoid saponins from Medicago hispida
inferred← citeshttps://doi.org/10.1016/0031-9422(91)83239-hopenalex-snapshot
A triterpenoid saponin from Oxytropis bicolor
inferred← citeshttps://doi.org/10.1016/0031-9422(91)83477-3openalex-snapshot
Saponins from Albizzia lucida
inferred← citeshttps://doi.org/10.1016/0031-9422(91)83478-4openalex-snapshot
Glycosides of ergosterol derivatives from Hericum erinacens
inferred← citeshttps://doi.org/10.1016/0031-9422(91)85099-lopenalex-snapshot
Structure—activity relationships of synthetic diosgenyl monoglycosides
inferred← citeshttps://doi.org/10.1016/0031-9422(91)85128-mopenalex-snapshot
Three saponins from Oxytropis species
inferred← citeshttps://doi.org/10.1016/0031-9422(91)85129-nopenalex-snapshot
Triterpene saponins from Cylicodiscus gabunensis
inferred← citeshttps://doi.org/10.1016/0031-9422(92)80073-nopenalex-snapshot
A triterpenoid saponin from Zygophyllum propinquum
inferred← citeshttps://doi.org/10.1016/0031-9422(92)80288-popenalex-snapshot
Steroidal saponins from the rhizomes of Smilax menispermoidea
inferred← citeshttps://doi.org/10.1016/0031-9422(92)80310-bopenalex-snapshot
Triterpenoid saponins from roots of Clematis grata
inferred← citeshttps://doi.org/10.1016/0031-9422(92)83294-9openalex-snapshot
A γ-pyronyl-triterpenoid saponin from Pisum sativum
inferred← citeshttps://doi.org/10.1016/0031-9422(92)83297-copenalex-snapshot
A dammarane saponin from Neoalsomitra integrifoliola
inferred← citeshttps://doi.org/10.1016/0031-9422(92)83298-dopenalex-snapshot
Cycloartane-type sapogenins and their glycosides from Curculigo orchioides
inferred← citeshttps://doi.org/10.1016/0031-9422(92)83469-fopenalex-snapshot
Steroidal saponins from Smilax lebrunii
inferred← citeshttps://doi.org/10.1016/0031-9422(92)83496-lopenalex-snapshot
Structure-activity relationships of synthetic diosgenyl diglycosides
inferred← citeshttps://doi.org/10.1016/0031-9422(92)83626-aopenalex-snapshot
Scammonins VII and VIII, two resin glycosides from Convolvulus scammonia
inferred← citeshttps://doi.org/10.1016/0031-9422(92)83678-ropenalex-snapshot
NMR Spectroscopy in the structural elucidation of oligosaccharides and glycosides
inferred← citeshttps://doi.org/10.1016/0031-9422(92)90068-2openalex-snapshot
A spirostanol glycoside from Yucca aloifolia
inferred← citeshttps://doi.org/10.1016/0031-9422(93)85048-vopenalex-snapshot
Minor steroidal glycosides from the roots of Smilax lebrunii
inferred← citeshttps://doi.org/10.1016/0031-9422(93)85108-4openalex-snapshot
Flavonoids from Pyracantha coccinea roots
inferred← citeshttps://doi.org/10.1016/0031-9422(93)85113-6openalex-snapshot
Triterpenoid glycosides from Stauntonia hexaphylla
inferred← citeshttps://doi.org/10.1016/0031-9422(93)85243-kopenalex-snapshot
Triterpenoids and their glycosides from Terminalia chebula
inferred← citeshttps://doi.org/10.1016/0031-9422(93)85244-lopenalex-snapshot
Symphytoxide A, A triterpenoid saponin from the roots of Symphytum officinale
inferred← citeshttps://doi.org/10.1016/0031-9422(93)85301-7openalex-snapshot
Anthraquinone and naphthalene glycosides from Rhamnus nakaharai
inferred← citeshttps://doi.org/10.1016/0031-9422(93)85357-wopenalex-snapshot
Triterpenoid oligoglycosides from Chionodoxa luciliae
inferred← citeshttps://doi.org/10.1016/0031-9422(93)85371-wopenalex-snapshot
Flavonoids and a saponin from Spartium junceum
inferred← citeshttps://doi.org/10.1016/0031-9422(93)85534-xopenalex-snapshot
Nortriterpenoid oligoglycosides from Chionodoxa luciliae
inferred← citeshttps://doi.org/10.1016/0031-9422(93)85538-3openalex-snapshot
Saponins from Zygophyllum propinquum
inferred← citeshttps://doi.org/10.1016/0031-9422(93)85546-4openalex-snapshot
Three flavone glycosides from Gelonium multiflorum
inferred← citeshttps://doi.org/10.1016/0031-9422(94)00716-7openalex-snapshot
Glycosides from Aster yunnanensis
inferred← citeshttps://doi.org/10.1016/0031-9422(94)00737-eopenalex-snapshot
(20R)-O-(3)-α-l-arabinopyranosyl-pregn-5-en-3β,20-diol from Brucea javanica
inferred← citeshttps://doi.org/10.1016/0031-9422(94)00744-eopenalex-snapshot
Triterpenoid saponins from Aster batangensis
inferred← citeshttps://doi.org/10.1016/0031-9422(94)00794-topenalex-snapshot
Triterpene saponins from Aster yunnanensis
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00016-zopenalex-snapshot
Medicagenic acid saponins from Aster batangensis
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00056-dopenalex-snapshot
Malabaricane triterpene glucosides from Adesmia aconcaguensis
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00181-6openalex-snapshot
Cyclohexyl butenolide glucosides from epacridaceae
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00246-4openalex-snapshot
A bidesmosidic hederagenin hexasaccharide from the roots of Symphytum officinale
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00690-7openalex-snapshot
Triterpenoid saponins of Mimusops elengi
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00782-2openalex-snapshot
Triterpenoid saponins from Gymnema sylvestre
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00936-1openalex-snapshot
Dammarane-type triterpenoid saponins from Bacopa monniera
inferred← citeshttps://doi.org/10.1016/0031-9422(96)00036-2openalex-snapshot
Matesaponin 5, a highly polar saponin from Ilex paraguariensis
inferred← citeshttps://doi.org/10.1016/0031-9422(96)00065-9openalex-snapshot
Biosynthesis of cyanohydrin glucosides from unnatural nitriles in intact tissue of Passiflora morifolia and Turnera angustifolia
inferred← citeshttps://doi.org/10.1016/0031-9422(96)00228-2openalex-snapshot
Steroidal glycosides from the subterranean parts of Liriope spicata var. prolifera
inferred← citeshttps://doi.org/10.1016/0031-9422(96)00247-6openalex-snapshot
An echinocystic acid saponin derivative from Kalimeris shimadae
inferred← citeshttps://doi.org/10.1016/0031-9422(96)00250-6openalex-snapshot
Bacopasaponin D-A pseudojujubogenin glycoside from Bacopa monniera
inferred← citeshttps://doi.org/10.1016/0040-4020(79)85038-3openalex-snapshot
13C nmr study of α- and β-anomeric pairs of d-mannopyranosides and l-rhamnopyranosides
inferred← citeshttps://doi.org/10.1016/0040-4020(95)00775-4openalex-snapshot
Downeyoside A and B, Two New Sulphated Steroid Glucuronides from the Starfish Henricia downeyae
inferred← citeshttps://doi.org/10.1016/0040-4039(82)80149-4openalex-snapshot
A new disaccharide, glaucobiose from Chinese drug “Pai-ch'ien”: A comparison of 13C NMR with its diastereomeric isomer, strophanthobiose
inferred← citeshttps://doi.org/10.1016/0040-4039(84)80117-3openalex-snapshot
Five new steroidal glycosides, pregnedioside-A, -B, and their three monoacetates, from an Okinawan soft coral of Alcyonium sp.
inferred← citeshttps://doi.org/10.1016/0045-2068(91)90025-kopenalex-snapshot
Monosaccharide acceptor substrate specificity of dextransucrase
inferred← citeshttps://doi.org/10.1016/0079-6565(82)80010-1openalex-snapshot
The determination of absolute configuration using nuclear magnetic resonance techniques
inferred← citeshttps://doi.org/10.1016/0079-6565(92)80011-4openalex-snapshot
13C NMR spectroscopy of oleanane triterpenoids
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00845-4openalex-snapshot
8.29 Spectroscopic Analysis: Diastereomeric Derivatization for Spectroscopy
inferred← citeshttps://doi.org/10.1016/b978-0-12-507701-9.50012-7openalex-snapshot
Nuclear Magnetic Resonance Analysis Using Chiral Derivatives
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00010-xopenalex-snapshot
Spectroscopic Analysis: Diastereomeric Derivatization for Spectroscopy
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.110624openalex-snapshot
Opeturins I-XIV, structurally diverse resin glycosides from Operculina turpethum and their biological activities
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.10.010openalex-snapshot
Structure and biological evaluation of novel cytotoxic sterol glycosides from the marine red alga Peyssonnelia sp.
inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.12.057openalex-snapshot
Anti-influenza diarylheptanoids from the bark of Alnus japonica
inferred← citeshttps://doi.org/10.1016/j.bse.2007.09.005openalex-snapshot
Chemical constituents from the leaves of Drypetes gerrardii
inferred← citeshttps://doi.org/10.1016/j.bse.2007.12.008openalex-snapshot
Chemical constituents of Scutellaria linearis
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