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1270960

CCOC(=O)c1cc(OC)c(F)c(F)c1F
Reaction #10371
title compound
Ausbeute 96.8%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)C(=C1CN(C(c2ccc(Cl)cc2)c2ccc(Cl)cc2)C1)c1cccc(C(=O)NN2CCCCC2)c1
Reaction #53466
1-[bis-(4-chlorophenyl)methyl]-3-{(methylsulfonyl)[3-(N-piperidylcarbamoyl)phenyl]methylene}azetidine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(NC(=O)c2ccccc2C(=C2CN(C(c3ccc(Cl)cc3)c3ccc(Cl)cc3)C2)S(C)(=O)=O)CC1
Reaction #53468
1-[bis(4-chlorophenyl)methyl]-3-{(methylsulfonyl)[(N-4-methylpiperazinylcarbamoyl)phenyl]methylene}azetidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #81364
N-(1,1-dimethylethoxycarbonyl)phenylalanine pentafluorophenyl ester
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(N3CCOCC3)c(F)c2)c(COc2ccc(F)c(F)c2)n1
Reaction #84521
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(Oc2cc(F)c(F)c(F)c2)CCCNC1=S
Reaction #158355
ethyl (3S)-2-thioxo-3-(3,4,5-trifluorophenoxy)piperidine-3-carboxylate
Ausbeute 142.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(Oc2cc(F)c(F)c(F)c2)CCCN=C1SC
Reaction #158356
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cc1cc(F)c(F)c(F)c1O
Reaction #158399
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1cc(F)c(F)c(F)c1O
Reaction #158400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1cc(F)c(F)c(F)c1OC1(C(=O)OCC)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158401
title compound
Ausbeute 45.2%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1cc(F)c(F)c(F)c1[N+](=O)[O-]
Reaction #160620
titled product
DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1cc(F)c(F)c(Nc2ccc(I)cc2F)c1[N+](=O)[O-]
Reaction #160621
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)C(C)(C)NC(=O)OCC1c2ccccc2-c2ccccc21)C(C)C
Reaction #161951
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methylalanyl-N-[(3R,4S,5S)-3-methoxy-5-methyl-1-oxo-1-(pentafluorophenoxy)heptan-4-yl]-N-methyl-L-valinamide
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(C)C
Reaction #161983
#174
Ausbeute 92.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)NCCC1C=CC=CC=C1)OC)N(C)C(=O)[C@@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(C)C
Reaction #161984
#175
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)[C@@]1(C)CCCN1C)C(C)C
Reaction #161992
compound #197
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)[C@]1(C)CCCN1C)C(C)C
Reaction #161995
compound #204
Ausbeute 125.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=NOC(CONC(=O)c2ccccc2NCc2ccncc2)C1
Reaction #176372
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(OCC2CC(F)CN2C(=O)Cc2ccc(NC(=O)Nc3ccccc3C)c(OC)c2)c(OC)c1
Reaction #177121
DOI: 10.1039/C8SC04228D
CC(C)(C)NC(=O)C1CCCCC1CC(O)C(Cc1ccccc1)NC(=O)C(CC(N)=O)NC(=O)OCc1ccccc1
Reaction #184763
DOI: 10.1039/C8SC04228D
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