Recherche de Sous-structure

215727

Cc1nc2ccc([C@@H]3C[C@H]3c3ccccc3)cc2c(N2CCOCC2)c1S(C)(=O)=O
Reaction #41938
white crystals
Rendement 61.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)CC=C(c2ccc(OC)cc2[N+](=O)[O-])CC1
Reaction #60419
1-(4,4-Diethylcyclohex-1-enyl)-4-methoxy-2-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
COC1CCN(c2ccc([N+](=O)[O-])c(C3=CC(C)(C)CC(C)(C)C3)c2)CC1
Reaction #60426
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc([N+](=O)[O-])c1C1=CC(C)(C)CC(C)(C)C1
Reaction #60467
title compound
Rendement 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c(C2=CC(C)(C)CC(C)(C)C2)c1
Reaction #60491
title compound
Rendement 34.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C2=CC(C)(C)CC(C)(C)C2)c([N+](=O)[O-])cc1OC
Reaction #60497
title compound
Rendement 85.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2cc([N+](=O)[O-])ccc2N2CCN(C(=O)OC(C)(C)C)CC2)CC(C)(C)C1
Reaction #60502
title compound
Rendement 14.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2c(F)cccc2[N+](=O)[O-])CC(C)(C)C1
Reaction #60514
title compound
Rendement 81.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2ccc(F)cc2C2CCN(C(=O)OC(C)(C)C)CC2)CC(C)(C)C1
Reaction #60544
title compound
Rendement 48.3%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1ccc(C(=O)OC)c(C)c1
Reaction #70187
4-Isopropenyl-2-methyl-benzoic acid methyl ester
Rendement 88.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1cnc(N2CCC(c3ccc(COc4ccc(S(C)(=O)=O)cc4)nc3)CC2)nc1
Reaction #70442
title compound
Rendement 79.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCC2CC1(O)C2(C)C.C[C@H](CCCCBr)B([O-])[O-]
Reaction #81912
pinanediol (R)-5-bromo-1-methylpentylboronate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC=C(c2ccc3cc(O)ccc3n2)CC1
Reaction #84074
methyl 4-(6-hydroxyquinolin-2-yl)cyclohex-3-enecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC=C(c2nc3ccc(OC)cc3cc2Cl)CC1
Reaction #84088
ethyl 4-(3-chloro-6-methoxyquinolin-2-yl)cyclohex-3-enecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1cncc(Br)c1
Reaction #86090
3-bromo-5-isopropenyl-pyridine
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1ccc(F)cc1[N+](=O)[O-]
Reaction #88140
4-fluoro-2-nitro-1-(prop-1-en-2-yl)benzene
Rendement 78.7%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)n(CCCO)c(=O)c2c(Cc3ccc(Cl)cc3)c(Cc3cccc(OC(F)(F)F)c3)cnc21
Reaction #88787
6-(3-(trifluoromethoxy)benzyl)-5-(4-chlorobenzyl)-3-(3-hydroxy propyl)-1-methylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione
Rendement 16.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@]1(C(=O)NC(C)(C)C)CCO[C@@H]1CCCB1OC(C)(C)C(C)(C)O1
Reaction #89628
(2R,3S)-3-acetamido-N-tert-butyl-2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)tetrahydrofuran-3-carboxamide
Rendement 63.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CCO[C@@H]1CCCB(O)O
Reaction #89629
(2R,3S)-3-amino-2-(3-boronopropyl)tetrahydrofuran-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(Cc2ccnc3ccccc23)C[C@@H]1CCCB(O)O
Reaction #89643
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(quinolin-4-ylmethyl)pyrrolidine-3-carboxylic acid
Rendement 27.4%DOI: 10.6084/m9.figshare.5104873.v1
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