tritert-butylphosphane

C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #202
Rendement 35.7%750 AstraZeneca ELN dataset
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #204
Rendement 31.5%750 AstraZeneca ELN dataset
c1cncc(N2CCNCC2)c1
Reaction #216
Rendement 0.0%750 AstraZeneca ELN dataset
CC(=O)Nc1cnc(N2CCN(C)CC2)cn1
Reaction #299
Rendement 79.5%750 AstraZeneca ELN dataset
CC(C)(C)OC(=O)NCCC1CCN(c2ccccc2)CC1
Reaction #317
Rendement 0.0%750 AstraZeneca ELN dataset
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #365
Rendement 15.0%750 AstraZeneca ELN dataset
COc1cc(Nc2ncc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-n1cnc(C)c1
Reaction #366
Rendement 0.0%750 AstraZeneca ELN dataset
COc1nc(Nc2ccc3c(n2)O[C@H](c2ccccc2)CN(C)C3)ccc1-c1cnn(C)c1
Reaction #440
Rendement 0.0%750 AstraZeneca ELN dataset
COc1nc(Nc2ccc3c(n2)OC(CC(F)(F)F)CN(C)C3)ccc1-c1cnn(C)c1
Reaction #506
Rendement 50.0%750 AstraZeneca ELN dataset
COc1nc(Nc2ccc3c(n2)OC(CC(F)(F)F)CN(C)C3)ccc1-c1cnn(C)c1
Reaction #507
Rendement 85.3%750 AstraZeneca ELN dataset
COC(=O)c1cc(Nc2ccccc2)cc(B2OC(C)(C)C(C)(C)O2)c1
Reaction #597
Rendement 2.3%750 AstraZeneca ELN dataset
COC(=O)c1cc(Nc2ccccc2)cc(B2OC(C)(C)C(C)(C)O2)c1
Reaction #598
Rendement 0.0%750 AstraZeneca ELN dataset
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(O)cc1
Reaction #760
Rendement 0.0%750 AstraZeneca ELN dataset
C[C@@H]1CN(c2ccc(S(C)(=O)=O)cc2)CCN1C(=O)OC(C)(C)C
Reaction #787
Rendement 0.0%750 AstraZeneca ELN dataset
FC1(F)Oc2ccc(N3CCNCC3)cc2O1
Reaction #802
Rendement 50.7%750 AstraZeneca ELN dataset
COc1ccc(N2CCN(C(=O)OC(C)(C)C)[C@H](C(C)C)C2)cc1OC
Reaction #813
Rendement 90.5%750 AstraZeneca ELN dataset
CN1CCN(c2ccc3[nH]ccc3c2)CC1
Reaction #8433
product
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=Cc1nc2cc(-c3ccc(C#N)cc3)ccc2o1
Reaction #10502
4-(2-vinyl-benzooxazol-5-yl)-benzonitrile
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cncc2cccc(N[C@H]3CC[C@@H](NC(=O)OC(C)(C)C)CC3)c12
Reaction #10652
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cncc2cccc(N[C@H]3CC[C@H](NC(=O)OC(C)(C)C)CC3)c12
Reaction #10654
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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