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1H-Azepine-1-carboxylic acid, hexahydro-3-hydroxy-4,5,6-tris(phenylmethoxy)-, phenylmethyl ester, (3R,4R,5R,6S)-

Base Information
  • Chemical Name:1H-Azepine-1-carboxylic acid, hexahydro-3-hydroxy-4,5,6-tris(phenylmethoxy)-, phenylmethyl ester, (3R,4R,5R,6S)-
  • CAS No.:924895-17-0
  • Molecular Formula:C35H37NO6
  • Molecular Weight:567.682
  • Hs Code.:
1H-Azepine-1-carboxylic acid,
hexahydro-3-hydroxy-4,5,6-tris(phenylmethoxy)-, phenylmethyl ester,
(3R,4R,5R,6S)-

Synonyms:

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Chemical Property of 1H-Azepine-1-carboxylic acid, hexahydro-3-hydroxy-4,5,6-tris(phenylmethoxy)-, phenylmethyl ester, (3R,4R,5R,6S)-
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Technology Process of 1H-Azepine-1-carboxylic acid, hexahydro-3-hydroxy-4,5,6-tris(phenylmethoxy)-, phenylmethyl ester, (3R,4R,5R,6S)-

There total 6 articles about 1H-Azepine-1-carboxylic acid, hexahydro-3-hydroxy-4,5,6-tris(phenylmethoxy)-, phenylmethyl ester, (3R,4R,5R,6S)- 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:
6-azido-2,3,4-tri-O-benzyl-6-deoxy-α,β-D-glucopyranose; In tetrahydrofuran; at 40 ℃;
With sodium cyanoborohydride; acetic acid; at 20 ℃; for 14h;
benzyl chloroformate; With potassium carbonate; In water; ethyl acetate; at 0 - 20 ℃;
DOI:10.1039/c3cc46646a
Guidance literature:
Multi-step reaction with 2 steps
1: 3.33 g / sodium cyanoborohydride / acetic acid / 6 h / 20 °C
2: 92 percent / KHCO3 / H2O; ethyl acetate / 20 °C
With sodium cyanoborohydride; potassium hydrogencarbonate; In water; acetic acid; ethyl acetate;
DOI:10.1039/b610377d
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