Nothing Special   »   [go: up one dir, main page]

Lunn et al., 1962 - Google Patents

Studies on the structure of catalposide

Lunn et al., 1962

View PDF
Document ID
16405574646115377333
Author
Lunn W
Edward D
Edward J
Publication year
Publication venue
Canadian Journal of Chemistry

External Links

Snippet

Catalposide extracted from the unripe fruit of Catalpa ovata affords bisdesoxyaucubin on reduction with lithium in liquid ammonia. The reduction is accompanied by the shift of a double bond. From this and other evidence, two possible structures are proposed for the …
Continue reading at cdnsciencepub.com (PDF) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/20Carbocyclic rings
    • C07H15/24Condensed ring systems having three or more rings
    • C07H15/256Polyterpene radicals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C08B37/0006Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
    • C08B37/0009Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
    • C08B37/0012Cyclodextrin [CD], e.g. cycle with 6 units (alpha), with 7 units (beta) and with 8 units (gamma), large-ring cyclodextrin or cycloamylose with 9 units or more; Derivatives thereof
    • C08B37/0015Inclusion compounds, i.e. host-guest compounds, e.g. polyrotaxanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C08B37/0006Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
    • C08B37/0045Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Galacturonans, e.g. methyl ester of (alpha-1,4)-linked D-galacturonic acid units, i.e. pectin, or hydrolysis product of methyl ester of alpha-1,4-linked D-galacturonic acid units, i.e. pectinic acid; Derivatives thereof
    • C08B37/0048Processes of extraction from organic materials

Similar Documents

Publication Publication Date Title
Van Cleve et al. The Structure of NRRL B-512 Dextran. Methylation Studies2
DE2560550C2 (en) Benzoquinone derivatives, processes for their preparation and medicaments containing them
Beroza Alkaloids from Tripterygium wilfordii Hook. The structure of wilforine, wilfordine, wilforgine and wilfortrine
Mayo et al. Helminthosporal, the toxin from Helminthosporium sativum: I. Isolation and characterization
Dickel et al. The Alkaloids of Tabernanthe iboga. Part III. 1 Isolation Studies
Beroza Pyrethrum synergists in sesame oil. Sesamolin, a potent synergist
El Khadem et al. 675. Constituents of the leaves of Psidium guaijava, L. Part II. Quercetin, avicularin, and guaijaverin
Miyano Rotenoids. XX. 1 Total synthesis of rotenone
Fales et al. Alkaloids of the Amaryllidaceae. VIII. The Structures of Narcissamine, Pseudolycorine and Methylpseudolycorine1
Lunn et al. Studies on the structure of catalposide
Francis et al. 2-Hydroxymethyl-3-methylquinoxaline 1: 4-dioxide: a metabolite of 2: 3-dimethylquinoxaline 1: 4-dioxide active against gram-negative bacteria
Pratt et al. Proof of the Structure of Sedoheptulosan as 2, 7-Anhydro-β-D-altroheptulopyranose1
Wyler et al. Cyclodopa glucoside (=(2S)‐5‐(β‐D‐glocopyranosyloxy)‐6‐hydroxyindoline‐2‐carboxylic acid) and its occurrence in red beet (beta vulgaris var. rubra L.)
Ham et al. Structural studies on glaucarubin from Simarouba glauca
Yunusov et al. The structure of talatisamine
Guise et al. Further constituents of Alphitonia species
Ayafor et al. Nkolbisine, a new furoquinoline alkaloid, and 7-deacetylazadirone from Teclea verdoorniana
Angyal et al. 267. Cyclitols. Part IV. Methyl ethers of myo inositol
US3110711A (en) Process of producing two escin isomers from horse chestnut extracts, and products
DE1287578B (en) Method for the temporary protection of carboxyl groups
Bobbitt et al. Catalpa Glycosides. I. The Characterization of Catalposide1
Andrews et al. Methylene Derivatives of L-Rhamnose1
Adams et al. Senecio alkaloids: the isolation of senecionine from Senecio cineraria and some observations on the structure of senecionine
Jurd Plant Polyphenols. VII. The Structure of Ellagorubin1
Kenner et al. 568. The degradation of carbohydrates by alkali. Part XIII. 2: 3-Di-O-methylglucose and its conversion into 5-hydroxymethylfurfuraldehyde