t-Butanol

Clc1ccc(N2CCOCC2)c(Cl)n1
Reaction #574
Ausbeute 0.0%750 AstraZeneca ELN dataset
O=S(=O)(c1ccco1)N1CCc2c(ccnc2Nc2cnc3ccccc3c2)C1
Reaction #763
Ausbeute 9.8%750 AstraZeneca ELN dataset
CCOC(=O)CCN1C(=O)C(N=[N+]=[N-])CCc2ccccc21
Reaction #1289
3-azido-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-propanoic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CCN1C(=O)C(N=[N+]=[N-])CCc2ccccc21
Reaction #1423
3-azido-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-propanoic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)Nc1ccc2c(c1)C(=O)c1ccccc1CO2
Reaction #1924
2-tert-butoxycarbonylamino-6,11-dihydrodibenz[b,e]oxepin-11-one
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)NC1(C(F)(F)F)CCN(Cc2ccccc2)C1
Reaction #1983
title compound
Ausbeute 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1cc(C2CC2)c2c(C)c(C3(NC(=O)OC(C)(C)C)CC3)c(F)cn2c1=O
Reaction #1996
1-cyclopropyl-8-(1-Bocamino-1-cyclopropyl)-7-fluoro-9-methyl-4-oxo-4H-quinolizine-3-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cccnc1C(=O)NC(C)(C)C
Reaction #2229
N-(1,1-dimethylethyl)-3-methyl-2-pyridine carboxamide
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1nc2cc(Cl)ccc2c(O)c1C(=O)OC
Reaction #3196
dimethyl 7-chloro-4-hydroxyquinoline-2,3-dicarboxylate
Ausbeute 28.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1nc2cccc(Cl)c2c(O)c1C(=O)OC
Reaction #3198
dimethyl 5-chloro-4-hydroxyquinoline-2,3-dicarboxylate
Ausbeute 80.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1nc2cc(Cl)cc(Cl)c2c(O)c1C(=O)OC
Reaction #3201
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1nc2cccc(C)c2c(O)c1C(=O)OC
Reaction #3202
title compound
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1nc2cccc(OC)c2c(O)c1C(=O)OC
Reaction #3211
desired compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)/C=C(\Nc1ccccc1C#N)C(=O)OC
Reaction #3214
solid
Ausbeute 44.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)NC(=O)c1cnccn1
Reaction #3742
N-tert-butyl-2-pyrazinecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)NC(=O)c1cnccn1
Reaction #3743
N-tert-butyl-2-pyrazine-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)NC(=O)c1cnccn1
Reaction #3744
N-tert-butyl-2-pyrazinecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(Cl)OC(=O)OC(C)(C)C
Reaction #4521
α-chloroethyl tert-butyl carbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)OCC(O)CN1CCCC1
Reaction #4603
oil
Ausbeute 82.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCOC(OCC)P(=O)(CC(CN)C1CCCCC1)OCC
Reaction #5279
ethyl 3-amino-2-cyclohexylpropyl(diethoxymethyl)phosphinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
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