N-(4-Phenylacetoxybenzyloxycarbonyl)-L-serine(O-2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)

Base Information

Chemical Name:N-(4-Phenylacetoxybenzyloxycarbonyl)-L-serine(O-2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)
CAS No.:182485-44-5
Molecular Formula:C₃₃H₃₈N₂O₁₅
Molecular Weight:702.669
Hs Code.:

Synonyms:N-(4-Phenylacetoxybenzyloxycarbonyl)-L-serine(O-2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)

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Chemical Property of N-(4-Phenylacetoxybenzyloxycarbonyl)-L-serine(O-2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)

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Technology Process of N-(4-Phenylacetoxybenzyloxycarbonyl)-L-serine(O-2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)

There total 2 articles about N-(4-Phenylacetoxybenzyloxycarbonyl)-L-serine(O-2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl) 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:

: 10378-06-0,20757-53-3,35954-65-5,123483-77-2,134308-33-1
2-methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[1,2-d]-2-oxazoline

: (S)-3-Hydroxy-2-(4-phenylacetoxy-benzyloxycarbonylamino)-propionic acid

: 182485-44-5
N-(4-Phenylacetoxybenzyloxycarbonyl)-L-serine(O-2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)

Guidance literature:

Reference yield:

: 3006-60-8,4539-83-7,6730-10-5,7772-79-4,7784-54-5,10385-50-9,14086-90-9,26151-16-6,76375-60-5,76375-61-6,95341-98-3,95341-99-4,134451-91-5,134451-96-0,136982-81-5,145375-11-7,148347-15-3
Acetic acid (2R,3R,4R,5S,6R)-2,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-4-yl ester

: 182485-44-5
N-(4-Phenylacetoxybenzyloxycarbonyl)-L-serine(O-2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)

Guidance literature:: Multi-step reaction with 2 steps

1: BF₃*Et₂O, 4 Angstroem molecular sieves / CH₂Cl₂ / 24 h / Ambient temperature

2: Et₃N / CH₂Cl₂; acetonitrile / 0.07 h / Ambient temperature

With 4 A molecular sieve; boron trifluoride diethyl etherate; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1021/ja970709e