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2-amino-3,4,6-tri-O-benzyl-2-deoxy-1-O-2-N-(phenylmethan-yl-ylidene)-α-D-glucopyranose

Base Information Edit
  • Chemical Name:2-amino-3,4,6-tri-O-benzyl-2-deoxy-1-O-2-N-(phenylmethan-yl-ylidene)-α-D-glucopyranose
  • CAS No.:459146-96-4
  • Molecular Formula:C34H33NO5
  • Molecular Weight:535.64
  • Hs Code.:
  • Mol file:459146-96-4.mol
2-amino-3,4,6-tri-O-benzyl-2-deoxy-1-O-2-N-(phenylmethan-yl-ylidene)-α-D-glucopyranose

Synonyms:2-amino-3,4,6-tri-O-benzyl-2-deoxy-1-O-2-N-(phenylmethan-yl-ylidene)-α-D-glucopyranose

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Chemical Property of 2-amino-3,4,6-tri-O-benzyl-2-deoxy-1-O-2-N-(phenylmethan-yl-ylidene)-α-D-glucopyranose Edit
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Technology Process of 2-amino-3,4,6-tri-O-benzyl-2-deoxy-1-O-2-N-(phenylmethan-yl-ylidene)-α-D-glucopyranose

There total 3 articles about 2-amino-3,4,6-tri-O-benzyl-2-deoxy-1-O-2-N-(phenylmethan-yl-ylidene)-α-D-glucopyranose 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:
Guidance literature:
3,4,6-tri-O-benzyl-D-glucal; With thianthrene-5-oxide; trifluoromethanesulfonic acid anhydride; In dichloromethane; chloroform; at -78 ℃; for 0.2h;
N-trimethylsilylbenzamide; With N,N-diethylaniline; In dichloromethane; chloroform; at 23 ℃; for 10h;
DOI:10.1021/ja026281n
Guidance literature:
3,4,6-tri-O-benzyl-D-glucal; benzamide; With N-iodo-succinimide; at -75 - 20 ℃; for 56h;
With sodium hydride; In dichloromethane; at 25 ℃; for 24h; Further stages.;
DOI:10.1016/j.tetlet.2004.06.082
Guidance literature:
3,4,6-tri-O-benzyl-D-glucal; benzamide; With N-iodo-succinimide; at -75 - 20 ℃; for 56h;
With 15-crown-6; sodium hydride; In dichloromethane; at 25 ℃; for 2h; Further stages.;
DOI:10.1016/j.tetlet.2004.06.082
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