بحث البنية الفرعية

COCC(C)N

COCCOCOc1ccc(C[C@H](NC(=O)OC(C)(C)C)C(=O)OC)cc1
Reaction #5822
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #40695
crude product
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
CCO[C@@H]1CN(C(=O)OC(C)(C)C)[C@@H](CO)CO1
Reaction #48618
desired compound
المردود 92.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1ccccc1)[C@H](O)[C@H]1CO[C@@H](CCC2CCCCC2)CN1C(=O)OC(C)(C)C
Reaction #48650
title compound
المردود 54.8%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
المردود 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
المردود 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
المردود 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
المردود 42.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1CSC(C(C)NC(=O)Cc2cc(F)cc(F)c2)=N1
Reaction #51292
title compound
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
المردود 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
COc1ccc([C@@H](NC(=O)OC(C)(C)C)C(=O)O)cc1C
Reaction #61111
(R)-tert-butoxycarbonylamino-(4-methoxy-3-methyl-phenyl)-acetic acid
المردود 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(F)(F)CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1N
Reaction #71990
title compound
المردود 93.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](N)[C@H](OC)C2)cnc1C
Reaction #72050
title compound
المردود 74.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cnc(C)c(C(=O)OC)c3)C[C@H]2OC)nc1Cl
Reaction #72051
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(F)c2c(c1)OCC1CCCN21
Reaction #84384
title compound
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #84385
solid
المردود 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@@H](C)NCc1ccc(F)c([C@]23CO[C@@H](c4cnn(C)c4)C[C@H]2CSC(N)=N3)c1
Reaction #155619
product
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي