isopropyl 6-O-tert-butyldiphenylsilyl-2,3-di-O-methyl-β-L-gulopyranoside

Base Information

Chemical Name:isopropyl 6-O-tert-butyldiphenylsilyl-2,3-di-O-methyl-β-L-gulopyranoside
CAS No.:1107603-33-7
Molecular Formula:C₂₇H₄₀O₆Si
Molecular Weight:488.697
Hs Code.:

Synonyms:isopropyl 6-O-tert-butyldiphenylsilyl-2,3-di-O-methyl-β-L-gulopyranoside

Suppliers and Price of isopropyl 6-O-tert-butyldiphenylsilyl-2,3-di-O-methyl-β-L-gulopyranoside

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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 isopropyl 6-O-tert-butyldiphenylsilyl-2,3-di-O-methyl-β-L-gulopyranoside

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Technology Process of isopropyl 6-O-tert-butyldiphenylsilyl-2,3-di-O-methyl-β-L-gulopyranoside

There total 1 articles about isopropyl 6-O-tert-butyldiphenylsilyl-2,3-di-O-methyl-β-L-gulopyranoside 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: 92.0%

: 1107603-32-6
isopropyl 4-O-benzyl-6-O-tert-butyldiphenylsilyl-2,3-di-O-methyl-β-L-gulopyranoside

: 1107603-33-7
isopropyl 6-O-tert-butyldiphenylsilyl-2,3-di-O-methyl-β-L-gulopyranoside

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In ethyl acetate; at 20 ℃; for 12h;
DOI:10.1002/chem.200801414

Reference yield: 75.0%

: 1107603-33-7
isopropyl 6-O-tert-butyldiphenylsilyl-2,3-di-O-methyl-β-L-gulopyranoside

: 121238-27-5
2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl trichloroimidate

: 1107603-34-8
isopropyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-(1->4)-6-O-tert-butyldiphenylsilyl-2,3-di-O-methyl-β-L-gulopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere; Molecular sieve;
DOI:10.1002/chem.200801414