An 35 Reaktionen beteiligt

1331321

Fc1ccc(Br)c(F)c1Cl
Reaction #51442
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(C)OC(=O)NC1C=CC(Cl)CC1
Reaction #222758
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Fc1ccc(Br)c(F)c1Cl
Reaction #293739
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC1COC(=O)O1
Reaction #310498
1,2-butylene carbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_10
O=C1OCC(c2ccccc2)O1
Reaction #310499
1-phenylethylene carbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_10
CC(C)(CC(=O)N1CCN(CCO)CC1)SCc1ccccc1
Reaction #466276
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CC(C)(C)C(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)C(=O)[C@H]5C[C@H]5[C@H]4[C@@H]3[C@H](Cl)[C@H]3O[C@]32C1
Reaction #478350
7α-chloro-5,6β-epoxy-15β,16β-methylen-3β-pivaloyloxy-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(C)(C)C(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)C(=O)[C@H]5C[C@H]5[C@H]4[C@@H]3[C@H](Cl)[C@H]3O[C@]32C1
Reaction #478351
7α-Chloro-5,6β-epoxy-15β,16β-methylen-3β-pivaloyloxy-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C(C(F)(Cl)Cl)C(Cl)(Cl)Cl
Reaction #725694
product
Ausbeute 128.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_12
CC(C)(C)OC(=O)N[C@@H]1C=C[C@H](Cl)CC1
Reaction #986814
cis-1-(tert-butoxycarbonylamino)-4-chloro-2-cyclohexene
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
CC(C)(C)OC(=O)N[C@@H]1C=C[C@H](Cl)CC1
Reaction #986960
cis-1-(tert-butoxycarbonylamino)-4-chloro-2-cyclohexene
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
C[C@@H]1CC2=CC(=O)CC[C@@H]2[C@@H]2[C@@H]1[C@@H]1CCC(=O)[C@@]1(C)C[C@@H]2Cl
Reaction #987863
11β-chloro-7α-methyl-estr-4-ene-3,17-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
CC(C)(C)[Si](OCCOCCOCCOCCCl)(c1ccccc1)c1ccccc1
Reaction #1042791
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
C=CC=C.C=Cc1ccccc1
Reaction #1059486
butadiene-styrene copolymer
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_10
C=CC=C.C=Cc1ccccc1
Reaction #1060155
butadiene-styrene copolymer
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_10
CC1(C)COC(c2cc(F)c(F)c(Cl)c2F)=N1
Reaction #1168583
title compound
Ausbeute 59.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
Fc1ccc(Br)c(F)c1Cl
Reaction #1311051
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
O=C(NNC(=O)C(Cl)(Cl)Cl)c1cccc2ccccc12
Reaction #1365271
N-α-naphthoyl-N'-trichloroacetylhydrazine
Ausbeute 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_07
CC(C)(CC(=O)N1CCN(CCO)CC1)SCc1ccccc1
Reaction #1445009
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
Fc1ccc(Br)c(F)c1Cl
Reaction #1542669
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_01
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