Recherche de Sous-structure

747266

C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #202
Rendement 35.7%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #204
Rendement 31.5%
c1cncc(N2CCNCC2)c1
Reaction #216
Rendement 0.0%
CC(=O)Nc1cnc(N2CCN(C)CC2)cn1
Reaction #299
Rendement 79.5%
CC(C)(C)OC(=O)NCCC1CCN(c2ccccc2)CC1
Reaction #317
Rendement 0.0%
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #365
Rendement 15.0%
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #366
Rendement 0.0%
COc1nc(Nc2ccc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-c1cnn(C)c1
Reaction #440
Rendement 0.0%
COc1nc(Nc2ccc3c(n2)OC(CC(F)(F)F)CN(C)C3)ccc1-c1cnn(C)c1
Reaction #506
Rendement 50.0%
COc1nc(Nc2ccc3c(n2)OC(CC(F)(F)F)CN(C)C3)ccc1-c1cnn(C)c1
Reaction #507
Rendement 85.3%
COC(=O)c1cc(N2CCOCC2)cc2c1nc(C)n2Cc1cccc(C(F)(F)F)c1C
Reaction #582
Rendement 0.0%
COC(=O)c1cc(Nc2ccccc2)cc(B2OC(C)(C)C(C)(C)O2)c1
Reaction #597
Rendement 2.3%
COC(=O)c1cc(Nc2ccccc2)cc(B2OC(C)(C)C(C)(C)O2)c1
Reaction #598
Rendement 0.0%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(O)cc1
Reaction #760
Rendement 0.0%
C[C@@H]1CN(c2ccc(S(C)(=O)=O)cc2)CCN1C(=O)OC(C)(C)C
Reaction #787
Rendement 0.0%
FC1(F)Oc2ccc(N3CCNCC3)cc2O1
Reaction #802
Rendement 50.7%
COc1ccc(N2CCN(C(=O)OC(C)(C)C)[C@H](C(C)C)C2)cc1OC
Reaction #813
Rendement 90.5%
CCC(C)P(Cc1ccc2ccccc2c1-c1c(C)ccc2ccccc12)C(C)CC
Reaction #2496
2-di(1'-methylpropyl)phosphinomethyl-2'-methyl-1,1'-binaphthyl
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2ccccc2c1-c1c(CP(C(C)C)C(C)C)ccc2ccccc12
Reaction #2497
2-diisopropylphosphinomethyl-2'-methyl-1,1'-binaphthyl
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(Cc2ccoc2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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