formate

O=P([O-])([O-])[O-]
Reaction #7441
Phosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cccc(NC(=O)NCCNC2=NS(=O)(=O)N=C2N[C@@H](Cc2ccc(O)cc2)C(=O)OC(C)(C)C)c1
Reaction #46332
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CON=C(C(=O)NC1C(=O)N2C(C(=O)[O-])=C(COC(C)=O)CS[C@H]12)c1csc(N)n1.[Na+]
Reaction #56247
sodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylate
Ausbeute 0.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCOCCn1nc(CC)c(N)c1C(N)=O
Reaction #173066
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCC1CNCC1c1ccccc1
Reaction #173586
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc2[nH]nc(Cc3ccccc3F)c2c1
Reaction #173774
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(CN2CCC(N3C(=O)Nc4ccccc4C3c3cccc(O)c3)CC2)c1
Reaction #174316
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c[nH]c(=O)n(CCCCl)c1=O
Reaction #174336
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)c1ccc(N(Cc2ccc(N(C)C)cc2)C(=O)C2CCCc3c(O)cccc32)cc1
Reaction #175125
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccc(C#N)c1O
Reaction #175643
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(N2CCNCC2)c2nc(C)ccc2c1
Reaction #176057
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(-c2sc3cc(OC)ccc3c2-c2cccc(O)c2)cc1
Reaction #176249
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1C(=O)CCc2ccc(NC(=O)c3ccc(C(F)(F)F)cc3NC3CCNCC3)cc21
Reaction #176897
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Oc1ccc2[nH]nc(-c3cc4cc(OCCN5CCCCC5)ccc4[nH]3)c2c1
Reaction #177274
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN(CC)CCOc1c(OC)cc(N)cc1OC
Reaction #177342
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(N)ccc2c1cnn2C1CCCCO1
Reaction #177521
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCC2CNCCN12
Reaction #177780
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)c1ccc(Nc2ncnc3c2CCNC3)cc1
Reaction #178559
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)c1scc2c1CN(C(=O)OC(C)(C)C)C2
Reaction #178666
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1nc2c(C)cc(C)nc2n1Cc1ccc(N)cc1
Reaction #180737
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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