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4926

CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #1288
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1293
title product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1294
title product
Ausbeute 196.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #1422
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1429
title product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1430
title product
Ausbeute 196.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)c1ccccc1)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41314
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)Cc1ccccc1)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41315
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]-2-phenyl-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CCOCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #42355
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2ccc(C(=O)N[C@@H](Cc3cc(F)cc(F)c3)[C@H](O)CNCc3cccc(CC)c3)cc21
Reaction #42498
title compound
Ausbeute 17.9%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(NC(=O)[C@H](CS(=O)(=O)Cc2ccccc2OC(F)F)N[C@@H](c2ccc(F)cc2)C(F)(F)F)CC1
Reaction #45290
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)COC1O
Reaction #48692
desired compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO[C@H]1OCC(C)(C)C
Reaction #48693
desired compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO[C@H]1OCC1(F)CCCCC1
Reaction #48708
title compound
Ausbeute 31.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO[C@H]1OCC(C)(CF)CF
Reaction #48733
desired compound
Ausbeute 42.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2O)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52920
N-(2,6-dichlorobenzoyl)-4-(2-hydroxyphenyl)-L-phenylalanine methyl ester
Ausbeute 50.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2OCC#N)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52922
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(O)c1-c1ccc(C[C@H](NC(=O)c2c(Cl)cccc2Cl)C(=O)O)cc1
Reaction #52974
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)O)N(c1ccc(C#N)cc1)c1nc(N)nc(Cc2c(Cl)cccc2Cl)n1
Reaction #53329
methyl N-(4-cyanophenyl)-N-[4-amino-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]glycine
Ausbeute 19.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)C=C.CC(C)C[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](N)CCC(=O)O)C(=O)O
Reaction #60574
Glu-Asn-Leu vinylsulfone
DOI: 10.6084/m9.figshare.5104873.v1
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