Substructure Search

304

CC(C)(C)OC(=O)N[C@@H]1CCC[C@H](C(=O)Nc2cc(-c3cnn4c3CCCCC4)c(F)cn2)C1
Reaction #613
Yield 72.4%
CC1(C)Cc2ncc(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)n2C1
Reaction #622
Yield 80.0%
CC1(C)CCn2ncc(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)c2C1
Reaction #661
Yield 52.8%
CC1(C)Cc2c(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #663
Yield 35.1%
CC1(C)Cc2c(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #664
Yield 53.6%
CC(C)(C)OC(=O)N[C@@H]1CCC[C@H](C(=O)Nc2cc(-c3cnn4c3CCCC4)c(F)cn2)C1
Reaction #694
Yield 37.4%
CC1(C)Cc2c(-c3cc(NC(=O)[C@@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #743
Yield 84.4%
CN(C)C(=O)[C@H]1CC[C@@H]2NS(=O)(=O)N(C(=O)OC(C)(C)C)[C@@H]2C1
Reaction #92325
title compound
Yield 74.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #92326
monohydrate
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2nc(C(=O)NC3CC(C(=O)N(C)C)CCC3NC(=O)C(=O)Nc3ccc(Cl)cn3)sc2C1
Reaction #211715
DOI: 10.1039/C8SC04228D
CN1CCc2nc(C(=O)NC3CC(C(N)=O)CCC3NC(=O)c3cc4cc(Cl)ccc4[nH]3)sc2C1
Reaction #262265
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N[C@H]1CCC[C@@H](C(N)=O)C1
Reaction #333342
(cis-3-carbamoyl-cyclohexyl)-carbamic acid tert-butyl ester
Yield 74.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCC[C@@H](C#N)C1
Reaction #333343
cis-(3-cyano-cyclohexyl)-carbamic acid tert-butyl ester
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)C1CCC(N)C(NC(=O)OC(C)(C)C)C1
Reaction #371539
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCC(N2CCC(NC(=O)OCc3ccccc3)C2=O)C(N)C1
Reaction #394783
DOI: 10.1039/C8SC04228D
CON(C)C(=O)C1CCCC(NC(=O)OC(C)(C)C)C1
Reaction #499418
tert-butyl 3-([methoxy(methyl)amino]carbonyl}cyclohexylcarbamate
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)C1CCCC(N(C)C(=O)OC(C)(C)C)C1
Reaction #499419
tert-butyl N-[3-(N-methoxy-N-methyl-carbamoyl)cyclohexyl]-N-methylcarbamate
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)C1CCCC(C=O)C1
Reaction #499420
tert-butyl 3-formylcyclohexyl(methyl)carbamate
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@H]1CC[C@H](NC(=O)OCc2ccccc2)[C@H](NC(=O)OC(C)(C)C)C1
Reaction #546728
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@H]1CC[C@H](N)[C@H](NC(=O)OC(C)(C)C)C1
Reaction #546729
title compound
Yield 97.1%DOI: 10.6084/m9.figshare.5104873.v1
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