99603-81-3

Upstream product

• 67-56-1 methanol 
• 112693-26-2 C₃₇H₆₂O₁₇ 

Downstream Products

• 142466-31-7 methyl 4-O-benzyl-2,3-di-O-methyl-α-L-fucopyranoside 
• 142466-38-4 4-O-benzyl-2,3-di-O-methyl-α/β-L-fucopyranose 
• 220855-12-9 Acetic acid (3S,4R,5R,6S)-5-benzyloxy-3,4-dimethoxy-6-methyl-tetrahydro-pyran-2-yl ester 
• 220855-13-0 C₅₈H₇₀O₁₃ 
• 142466-43-1 methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-6-O-benzyl-2-deoxy-4-O-(4-O-benzyl-2,3-di-O-methyl-α-L-fucopyranosyl)-2-deoxy-β-D-glucopyranoside 
• 142466-47-5 methyl 2-acetamido-6-O-benzyl-4-O-(4-O-benzyl-2,3-di-O-methyl-α-L-fucopyranosyl)-2-deoxy-3-O-(3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 142466-39-5 (2S,3R,4R,5S)-3-Benzyloxy-6-bromo-4,5-dimethoxy-2-methyl-tetrahydro-pyran 

Relevant academic research and scientific papers

Comparative Studies on the Constituents of a Parasitic Plant and Its Host. III. On the Constituents of Boschniakia rossica FEDTSCH, et FLEROV. (2)

Two iridoid glucosides, namely boschnaloside (2), (+)-pinoresinol-β-D-glucopyranoside (3), a new oligosaccharide (=β-D-glucopyranosyl(1->4)-α-L-rhamnopyranosyl-(1->3)-D-(4-O-caffeoyl)-glucopyranose) (4), and a new phenylpropanoid glycoside named rossicaside A (5) have been isolated from Boschniakia rossica FEDTSCH, et FLEROV (Orobanchaceae) and their structures have been determined.Keywords--Boschniakia rossica; Orobanchaceae; boschnaloside; boschnaside; (+)-pinoresinol-β-D-glucoside; acetylated oligosaccharide; rossicaside A; phenylpropanoid glycoside

GLYCOSIDES OF MARINE INVERTEBRATES. XV. A NEW TRITERPENE GLYCOSIDE - HOLOTHURIN A1 - FROM CARIBBEAN HOLOTHURIANS OF THE FAMILY HOLOTHURIIDAE

A glycoside, holothurin A1 has been isolated from the polar glycosidic fractions of the holothurians H. floridana and H. grisea.The complete structure of the glycoside has been established; it is: 3β-3)-O-β-D-glucopyranosyl-(1->4)-O-β-D-quinovopyranosyl-(1->2)-(4-sulfato-β-D-xylopyranosyl)oxy>holosta-9(11)-ene-12α,17α,22ξ-triol.Details of the IR and 1H and 13C NMR spectra of the compounds obtained are given.