N-(chlorocarbonyl) isocyanate

C#CCn1c(=O)[nH]c(=O)n(-c2cc(NC(C)=O)c(F)cc2Cl)c1=O
Reaction #1577
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1oc(-c2ccc(C(F)(F)F)cc2)nc1-c1ccc(-c2ccc(Cn3oc(=O)[nH]c3=O)cc2)cc1
Reaction #75939
solid
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C#CCn1c(=O)[nH]c(=O)n(-c2cc(NC(C)=O)c(F)cc2Cl)c1=O
Reaction #80704
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cn1c(=O)[nH]c(=O)n(-c2ccc(Oc3nc4ccc(Cl)cc4s3)cc2)c1=O
Reaction #93227
1-[4-(6-chlorobenzothiazol-2-yloxy)phenyl]-3-methyl-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione
Ausbeute 72.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CC/C(=C\Cn1oc(=O)[nH]c1=O)c1cccc(OCc2nc(-c3ccc(C(F)(F)F)cc3)oc2C)c1
Reaction #216703
solid
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC/C(=C\Cn1oc(=O)[nH]c1=O)c1cccc(OCc2nc(-c3ccc(C(F)(F)F)cc3)oc2C)c1
Reaction #216704
solid
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
O=C(NC(=O)Nc1ccccc1Oc1ccccc1)Nc1nccs1
Reaction #218962
title compound
Ausbeute 55.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=c1[nH]c(=O)n(Cc2ccc(Oc3cccc(Oc4ccc(Cn5oc(=O)[nH]c5=O)cc4)c3)cc2)o1
Reaction #350722
1,3-bis[4-[(3,5-dioxo-1,2,4-oxadiazolidin-2-yl)methyl]phenoxy]benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
C#CCn1c(=O)[nH]c(=O)n(-c2cc(NC(C)=O)c(F)cc2Cl)c1=O
Reaction #450358
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
CC(C)(C)OC(=O)N[C@@H]1C(=O)N(OCc2ccccc2)[C@@H]1COC(N)=O
Reaction #502042
(3S,4S)-1benzyloxy-3-(tert-butoxycarbonylamino)-4-carbamoyloxymethyl-2azetidinone
Ausbeute 72.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
COC(=O)Cn1c(=O)[nH]c(=O)n(-c2cc(F)ccc2[N+](=O)[O-])c1=O
Reaction #527731
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
CCOC(=O)Cn1c(=O)[nH]c(=O)n(-c2cc(Oc3ccc(C(F)(F)F)c(Cl)c3)ccc2[N+](=O)[O-])c1=O
Reaction #527745
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
O=c1[nH]c(=O)c2c(o1)C(c1ccccc1)CC2
Reaction #538202
7-phenyl-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione
Ausbeute 13.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=c1[nH]c(=O)c2c(o1)C(c1ccc(F)cc1)CC2
Reaction #538216
7-(4-fluorophenyl)-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione
Ausbeute 52.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=c1[nH]c(=O)c2c(o1)C(c1ccccc1)COC2
Reaction #538240
8-phenyl-7,8-dihydropyrano[3,4-e][1,3]oxazine-2,4(3H,5H)-dione
Ausbeute 61.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=c1[nH]c(=O)c2c(o1)C(c1ccc(Cl)cc1)CC2
Reaction #538256
7-(4-chlorophenyl)-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione
Ausbeute 51.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=c1[nH]c(=O)c2c(o1)C(c1ccc(F)c(F)c1)CC2
Reaction #538260
7-(3,4-difluorophenyl)-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione
Ausbeute 51.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=c1[nH]c(=O)c2c(o1)C(c1cc(F)cc(F)c1)CC2
Reaction #538270
7-(3,5-difluorophenyl)-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione
Ausbeute 10.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=c1[nH]c(=O)c2c(o1)C(c1cc(F)c(F)c(F)c1)CC2
Reaction #538275
7-(3,4,5-trifluorophenyl)-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione
Ausbeute 46.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=c1[nH]c(=O)c2c(o1)C(c1ccc(F)cc1F)CC2
Reaction #538280
7-(2,4-difluorophenyl)-6,7-dihydrocyclopenta[e][1,3]oxazine-2,4(3H,5H)-dione
Ausbeute 36.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
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