(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-4-O-benzyl-2-O-levulinoyl-α/β-L-rhamnopyranose trichloroacetimidate

Base Information

Chemical Name:(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-4-O-benzyl-2-O-levulinoyl-α/β-L-rhamnopyranose trichloroacetimidate
CAS No.:1091625-33-0
Molecular Formula:C₅₄H₅₈Cl₃NO₁₂
Molecular Weight:1019.41
Hs Code.:

Synonyms:(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-4-O-benzyl-2-O-levulinoyl-α/β-L-rhamnopyranose trichloroacetimidate

Suppliers and Price of (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-4-O-benzyl-2-O-levulinoyl-α/β-L-rhamnopyranose trichloroacetimidate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-4-O-benzyl-2-O-levulinoyl-α/β-L-rhamnopyranose trichloroacetimidate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-4-O-benzyl-2-O-levulinoyl-α/β-L-rhamnopyranose trichloroacetimidate

There total 1 articles about (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-4-O-benzyl-2-O-levulinoyl-α/β-L-rhamnopyranose trichloroacetimidate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

: (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-4-O-benzyl-2-O-levulinoyl-α/β-L-rhamnopyranose

: 545-06-2
trichloroacetonitrile

: 1091625-33-0
(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-4-O-benzyl-2-O-levulinoyl-α/β-L-rhamnopyranose trichloroacetimidate

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In 1,2-dichloro-ethane; at -5 ℃; for 0.166667h; Inert atmosphere;
DOI:10.1002/ejoc.200800693

Reference yield: 92.0%

: 1091625-32-9
allyl (3,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-2-O-acetyl-4-O-benzyl-α-L-rhamnopyranoside

: 1091625-33-0
(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-4-O-benzyl-2-O-levulinoyl-α/β-L-rhamnopyranose trichloroacetimidate

: 1091625-38-5
allyl (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-(4-O-benzyl-2-O-levulinoyl-α-L-rhamnopyranosyl)-(1->2)-(3,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-2-O-acetyl-4-O-benzyl-α-L-rhamnopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In toluene; at -78 - 20 ℃; Molecular sieve;
DOI:10.1002/ejoc.200800693

Reference yield: 92.0%

: 1091625-33-0
(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-4-O-benzyl-2-O-levulinoyl-α/β-L-rhamnopyranose trichloroacetimidate

: 119471-45-3
allyl 3,4-di-O-benzyl-α-L-rhamnosylpyranose

: 1091625-50-1
allyl (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->3)-(4-O-benzyl-2-O-levulinoyl-α-L-rhamnopyranosyl)-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In toluene; at -78 - 20 ℃; for 0.25h; Molecular sieve;
DOI:10.1021/jo802127z