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CC(C)N

CC1(C)Cc2c(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #663
Выход 35.1%
CC1(C)Cc2c(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #664
Выход 53.6%
CC1(C)Cc2c(-c3cc(NC(=O)[C@@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #743
Выход 84.4%
C[C@@H](C(=O)O)N1CC[C@H](N(Cc2nccs2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7380
title compound
Выход 70.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1c[nH]c2c(OCc3ccccc3)cccc12)[N+](=O)[O-]
Reaction #8184
3-(2-methyl-2-nitropropyl)-7-(benzyloxy)indole
Выход 92.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8185
22.41
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)O)N1CC[C@H](N(Cc2nccs2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #61704
title compound
Выход 70.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2ncnc3c2c(-c2ccc(C(=O)Nc4cc(C(F)(F)F)ccn4)cc2)nn3[C@@H]2CCCc3c2cnn3S(=O)(=O)c2ccc(C)cc2)c(OC)c1
Reaction #90742
(R)-4-(4-((2,4-dimethoxybenzyl)amino)-1-(1-tosyl-4,5,6,7-tetrahydro-1H-indazol-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-N-(4-(trifluoromethyl)pyridin-2-yl)benzamide
Выход 87.4%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1c(-c1ccc(C(=O)Nc3cc(C(F)(F)F)ccn3)cc1)nn2[C@@H]1CCCc2[nH]ncc21
Reaction #90743
title compound
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(c1cc(C(=O)N2CCc3cc(F)ccc32)cc(N2CCC(n3c(=O)[nH]c4ncccc43)CC2)n1)S(C)(=O)=O
Reaction #161855
N-[4′-(5-fluoro-2,3-dihydro-indole-1-carbonyl)-4-(2-oxo-2,3-dihydro-imidazo[4,5-b]pyridin-1-yl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-6′-yl]-N-methyl-methanesulphonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)Oc2cc(=O)n(C)c3c2c(=O)n(C2CC2)c(=O)n3-c2cccc([N+](=O)[O-])c2)cc1
Reaction #162813
toluene-4-sulfonic acid 3-cyclopropyl-8-methyl-1-(3-nitrophenyl)-2,4,7-trioxo-1,2,3,4,7,8-hexahydro-pyrido[2,3-d]pyrimidin-5-yl ester
Выход 82.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)Oc2cc(=O)n(C)c3c2c(=O)n(C2CC2)c(=O)n3-c2cccc(N)c2)cc1
Reaction #162814
toluene-4-sulfonic acid 1-(3-aminophenyl)-3-cyclopropyl-8-methyl-2,4,7-trioxo-1,2,3,4,7,8-hexahydro-pyrido[2,3-d]pyrimidin-5-yl ester
Выход 75.8%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2c3cnc(Nc4ccc(N5CCNCC5)cn4)nc3n(C3CCCC3)c2n1
Reaction #166346
compound 270
Выход 108.2%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)ccc2c3cnc(Nc4ccc(N5CC[C@@H](O)C5)cn4)nc3n(C3CCCC3)c21
Reaction #166351
compound 275
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1OCC(=O)NC1c1cc(Br)cc([N+](=O)[O-])c1
Reaction #168740
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](COc1ccc(C(F)(F)F)cc1C(=O)/N=c1\sc(C(C)(C)C)cn1C[C@@H]1CCCO1)CO[Si](C)(C)C(C)(C)C
Reaction #169945
title compound
Выход 69.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cn(C[C@H]2CCCO2)/c(=N/C(=O)c2cc(C(F)(F)F)ccc2OC[C@H](N)CO)s1
Reaction #169957
title compound
Выход 74.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NC(=O)Nc1ccc([N+](=O)[O-])cc1O
Reaction #174570
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OC1CC(n2ccc3c(NCC4CC4)ncnc32)CC1COS(N)(=O)=O
Reaction #178443
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1Nc1ncc(Cl)c(NC3C4C=CC(C4)C3C(N)=O)n1)CCN(CC(C)(C)O)CC2
Reaction #188461
DOI: 10.1039/C8SC04228D
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