triphosgene

COc1ccc(CCN=C=O)cc1
Reaction #2933
4-methoxy-β-phenylethyl isocyanate
Rendimiento 0.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1[nH]c2cccc(Cl)c2c(=O)o1
Reaction #3197
title compound
Rendimiento 250.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc2[nH]c(=O)oc(=O)c12
Reaction #3209
title compound
Rendimiento 283.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1[nH]c2cc(C(F)(F)F)cc(Cl)c2c(=O)o1
Reaction #3226
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1sc(C)c2[nH]c(=O)[nH]c12
Reaction #5331
title compound
Rendimiento 4777.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(=O)N(C)c1ccccc1
Reaction #10029
pure compound
Rendimiento 70.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CC(=O)N(C)c1ccccc1
Reaction #10030
pure compound
Rendimiento 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CC(=O)N(C)c1ccccc1
Reaction #10031
N-methyl-N-phenylaminoacrolein
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CC(=O)N(C)c1ccccc1
Reaction #10033
N-methyl-N-phenylaminoacrolein
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)n1c(C=CC=O)c(-c2ccc(F)cc2)c2ccccc21
Reaction #10035
product
Rendimiento 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(CNC(=O)N4CCCCC4)c3C2=O)C(=O)N1
Reaction #10153
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4- yl]methyl}piperidylcarboxamide
Rendimiento 145.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)Nn1c(=O)c2cc(F)c(F)c(Cl)c2n(C2CC2)c1=O
Reaction #10407
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=c1[nH]c2cc(F)c(F)cc2c(=O)n1N(Cc1ccccc1)Cc1ccccc1
Reaction #10409
title compound
Rendimiento 198.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN(CCCc1ccncc1)C(=O)N(C)CCC12CC3CC(CC(C3)C1)C2
Reaction #11568
titled compound
Rendimiento 141.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCc1cccc(CNC[C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)N2CCC(CS(C)(=O)=O)CC2)c1
Reaction #42587
title compound
Rendimiento 7.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc2c(N3CCN(CCc4cccc(N5C[C@H]6CCCN6C5=O)c4)CC3)cccc2n1
Reaction #44175
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)C(=O)N[C@H]1CC[C@H](CCN2CCN(c3cccc(Cl)c3Cl)CC2)CC1
Reaction #44400
title compound
Rendimiento 143.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)C(=O)N(C2CCCN(C(N)=O)CC2)CC1COc1ccc(C#N)cn1
Reaction #44483
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)n1c(=O)n(C(=O)NCC2CCN(C(=O)OC(C)(C)C)CC2)c2ccccc21
Reaction #44872
oil
Rendimiento 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1c(F)c(I)c(C)c2c(=O)oc(=O)[nH]c12
Reaction #45568
7-Fluoro-6-iodo-8-methoxy-5-methyl-1H-benzo[d][1,3]oxazine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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