Substructure Search

CC(C)(C)N

COC(=O)C(CN1CCO[C@@H](CNC(=O)OC(C)(C)C)C1)c1c(F)cnc2ccc(OC)nc12
Reaction #43620
Racemic methyl 3-{(2S)-2-[({[(1,1-dimethylethyl)oxy]carbonyl}amino)methyl]-4-morpholinyl}-2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]propanoate
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)[C@@]1(C)CCNC1
Reaction #45913
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@]1(C)CCN(c2c(-c3cccc(F)c3)c(C)c(C#N)c3nc(C(=O)N(C)C)oc23)C1
Reaction #45916
compound
Yield 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@]1(C)CCN(c2c(-c3ccccc3)c(C)c(C#N)c3nc(C(=O)N(C)C)oc23)C1
Reaction #45917
compound
Yield 21.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1N(C(C)(C)C)C(=O)C1(NC(=O)Cc1ccccc1)[SiH](C)C
Reaction #179946
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCC(N)(CCO)C1
Reaction #185131
DOI: 10.1039/C8SC04228D
CCCCCCCCNC(=O)C12CCC(N(CC(=O)N3CC(F)CC3C#N)C(=O)OCc3ccccc3)(CC1)CC2
Reaction #185640
DOI: 10.1039/C8SC04228D
C#CC(C)(C)N1CCC(OC(=O)N(CC)c2ccccc2OC)N(c2nnc(C(F)(F)F)s2)C1=O
Reaction #188335
DOI: 10.1039/C8SC04228D
CCOc1cc(C(C)(C)C)ncc1C1=NC(C)(c2ccc(Cl)cc2)C(C)(c2ccc(Cl)cc2)N1C(=O)NC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #192309
DOI: 10.1039/C8SC04228D
CC(C)C1(C)N=C(c2nc3ccc(N=C=S)cc3cc2C(=O)O)NC1=O
Reaction #193199
DOI: 10.1039/C8SC04228D
COc1cc([N+](=O)[O-])ccc1S(=O)(=O)NC(C)(C)C
Reaction #198920
DOI: 10.1039/C8SC04228D
CCOc1cc(C(C)(C)C)ncc1C1=NC(C)(c2ccc(Cl)cc2)C(C)(c2ccc(Cl)cc2)N1C(=O)N1CCN(CC(=O)N2CCN(C)CC2)CC1
Reaction #205682
DOI: 10.1039/C8SC04228D
CCOc1cc(C(C)(C)C)ncc1C1=NC(C)(c2ccc(Cl)cc2)C(C)(c2ccc(Cl)cc2)N1C(=O)N1CCC(CC(=O)NCc2cc(C)cc(F)c2)CC1
Reaction #210960
DOI: 10.1039/C8SC04228D
CCCCCCNC(=O)C12CCC(N(CC(=O)N3CC(F)CC3C#N)C(=O)OCc3ccccc3)(CC1)CC2
Reaction #212724
DOI: 10.1039/C8SC04228D
CC1(C)CC(=O)CC(C)(C)N1OC1CCCCC1
Reaction #220813
title compound
Yield 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)CC(C)(C)N1OC1CCCCC1
Reaction #220828
title compound
Yield 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)CC(C)(C)N1OC1CCCCC1
Reaction #220837
title compound
Yield 732.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)CC(C)(C)N1OC1CCCCC1
Reaction #220845
title compound
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)CC(C)(C)N1OC1CCCCC1
Reaction #220846
title compound
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2=NC(C)(c3ccc(Cl)cc3)C(c3ccc(Cl)cc3)N2C(=O)NCCN(C)C)c(OC(C)C)c1
Reaction #223029
DOI: 10.1039/C8SC04228D
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