بحث البنية الفرعية

3314

N=C(NC(=O)OCC(Cl)(Cl)Cl)c1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4c(Cl)cc(Cl)cc4s3)C2=O)c1
Reaction #2848
title compound
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)OC(Cl)C(Cl)(Cl)Cl
Reaction #4526
1,2,2,2-tetrachloroethyl N-methylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCc2ccccc21
Reaction #5523
1-carbamylindoline
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCC1(O)CCc2ccccc2C12CCCC2)OCC(Cl)(Cl)Cl
Reaction #5638
title compound
المردود 78.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC(Cl)(Cl)Cl)N1CCc2ccccc2C1
Reaction #51099
title compound ( D6 )
المردود 99.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC(Cl)(Cl)Cl)N1CCC(=C2c3ccccc3Oc3ccccc32)CC1
Reaction #64888
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2C(C2CCN(C(=O)OCC(Cl)(Cl)Cl)CC2)c2ccccc21
Reaction #64890
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N(Cc2ccc(C)cc2)C(=O)OCC(Cl)(Cl)Cl)c2sc(NC(=O)c3ccccc3)nc12
Reaction #80142
(2-benzoylamino-4-methoxy-benzothiazol-7-yl)-(4-methyl-benzyl)-carbamic acid 2,2,2-trichloro-ethyl ester
المردود 40.4%DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](NC(=O)OCC(Cl)(Cl)Cl)C(=O)O
Reaction #81366
(2,2,2-trichloroethoxycarbonyl)lysine
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCc2ccccc21
Reaction #83614
1-carbamylindoline
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCc2ccccc21
Reaction #83615
1-carbamylindoline
المردود 270.4%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCc2ccccc21
Reaction #83618
1-carbamylindoline
المردود 248.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)OCC(Cl)(Cl)Cl)n(-c2ccc(Cl)c(OCCOC3CCCCO3)c2)n1
Reaction #88920
title compound
المردود 101.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(O[Si](C(C)C)(C(C)C)C(C)C)cc(-n2nc(C(C)(C)C)cc2NC(=O)OCC(Cl)(Cl)Cl)c1
Reaction #88924
title compound
المردود 103.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](Oc1ccc(-n2nc(C(C)(C)C)cc2NC(=O)OCC(Cl)(Cl)Cl)cc1CO)(C(C)C)C(C)C
Reaction #88933
title compound
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)OCC(Cl)(Cl)Cl)n(-c2cc(Cl)cc(O[Si](C)(C)C(C)(C)C)c2)n1
Reaction #88939
title compound
المردود 107.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)OCC(Cl)(Cl)Cl)n(-c2ccnc(OCCO)c2)n1
Reaction #88946
title compound
المردود 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1nn(CCOC2CCCCO2)cc1-n1nc(C(C)(C)C)cc1NC(=O)OCC(Cl)(Cl)Cl)(C(C)C)C(C)C
Reaction #88956
title compound
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)OCC(Cl)(Cl)Cl)n(-c2ccc(Cl)c(OCCCOC3CCCCO3)c2)n1
Reaction #88960
title compound
المردود 70.3%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C=C(C(=O)OCCC#N)C(=S)NC(=O)OCC(Cl)(Cl)Cl)CC
Reaction #95989
pure adduct
المردود 38.5%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي