#4524237

O=C(CNC(=O)OCc1ccccc1)Nn1cccc1
Reaction #50656
product
收率 18.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(=O)c1cccn1NC(=O)CNC(=O)OCc1ccccc1
Reaction #50681
product
收率 70.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=C(CNC(=O)OCc1ccccc1)Nn1ccc(C(=O)c2ccccc2)c1
Reaction #50686
Phenylmethyl-[2-[(3-benzoyl-1H-pyrrol-1-yl)amino]-2-oxoethyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
—
Reaction #63792
tripeptide ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COC(CN(CC(=O)O)C(=O)OCc1ccccc1)OC
Reaction #67526
product 37
收率 61.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
NCC(=O)Oc1ccc([N+](=O)[O-])cc1
Reaction #74710
glycine p-nitrophenyl ester
收率 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
O=C(CNC(=O)OCc1ccccc1)Oc1ccc2ccccc2c1
Reaction #74711
N-benzyloxycarbonyl glycine β-naphthyl ester
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
O=C(CNC(=O)OCc1ccccc1)OSc1ccccc1
Reaction #74712
N-benzyloxycarbonyl-glycine-phenythio ester
收率 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
O=C(CNC(=O)OCc1ccccc1)ON1C(=O)CCC1=O
Reaction #159280
Z-Gly-OSu
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #159332
benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)[C@H](NC(=O)CNC(=O)OCc1ccccc1)C(=O)NC[C@@H](O)CP(=O)(CC1CCCCC1)OCc1ccccc1
Reaction #159339
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C(Cc1ccccc1)NC(=O)CNC(=O)OCc1ccccc1
Reaction #188295
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CC(NC(=O)CNC(=O)OCc2ccccc2)C1
Reaction #188468
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)OCC1C(NC(=O)CNC(=O)OCc2ccccc2)CC2CN(C(=O)OC(C)(C)C)CC21
Reaction #196327
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)NC(=O)CN1C(=O)CNC(=O)OCc1ccccc1
Reaction #201410
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCC[C@H](CC(O)C(NC(=O)OCc1ccccc1)C(=O)O)O[Si](C)(C)C(C)(C)C
Reaction #216248
(2R/S,3R/S,5R)-2-[1-(benzyloxy)formamido]-5-(t-butyldimethylsiloxy)-3-hydroxyhexadecanoic acid
收率 47.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC(=O)OCC1C(NC(=O)CNC(=O)OCc2ccccc2)CC2CN(C(=O)OC(C)(C)C)CC21
Reaction #217562
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(C)(C)OC(=O)N1CCC(CNC(=O)CNC(=O)OCc2ccccc2)CC1
Reaction #220786
4-[[(N-(benzyloxycarbonyl) glycyl)amino]methyl]-1-(tert-butoxycarbonyl)piperidine
收率 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C(CNC(=O)OCc1ccccc1)Nn1cccc1
Reaction #222378
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C1(N(C)C(=O)CNC(=O)OCc2ccccc2)CC1
Reaction #227597
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
第 1 页下一页