#11206129

COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #909
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #910
title compound
収率 55.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccn(C)c1S(=O)(=O)NC(C)(C)C
Reaction #924
title compound
収率 14.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)NCCc1ccccc1
Reaction #1689
title compound
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)NNc1ccccc1OCCSC
Reaction #4340
2-[2-(methylthioethoxy)-phenyl]-hydrazinecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)N[C@@H](CO)C(C)C
Reaction #5035
N-Methyloxycarbonyl-D-valinol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)NCCSc1cccc2nccn12
Reaction #5544
desired product
収率 66.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)NCCSc1cccc2nccn12
Reaction #5579
desired product
収率 66.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)N(c1ccncc1)c1ccc2c(ccn2C)c1
Reaction #5988
solid
収率 98.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)N1CCC(C)CC1
Reaction #7309
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)Oc1ccc(F)cc1C
Reaction #7575
4-fluoro-2-methylphenyl methyl carbonate
収率 78.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)N[C@H]1CCN(c2ccc(N3C[C@H](CNc4ccon4)OC3=O)cc2F)C1
Reaction #8261
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)N[C@@H]1CCN(c2ccc(N3C[C@H](CN(C(=O)OCC(Cl)(Cl)Cl)c4ccon4)OC3=O)cc2F)C1
Reaction #8268
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)Nc1c(C(=O)c2cccnc2)oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc12
Reaction #8886
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)N[C@@H](C)CN1CC(C)(C)OC[C@H]1C(=O)Nc1cc(Cl)cc2c1[nH]c1cnccc12
Reaction #40505
desired product
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)NS(=O)(=O)c1ccccc1Cl
Reaction #40789
white solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)N[C@@H](C)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41285
Methyl ((1S,2R)-2-{[1-(4-fluorophenyl)-1H-indazol-5-yl]oxy}-1-methyl-2-phenylethyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC1(c2c[nH]c3c(NC(=O)OC)cccc23)CCc2cc(F)ccc21
Reaction #41991
title compound
収率 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)NCC1Cc2cc(Cl)c3ccccc3c2O1
Reaction #42220
(±)-methyl (5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methylcarbamate
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)NCC1Cc2c(Cl)cc3c(c2O1)CCC3
Reaction #42229
(±)-methyl (4-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methylcarbamate
収率 92.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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