Busqueda de Subestructura

CC(C)OC(C)C

CCc1cc(N[C@H]2CC[C@@H](C(C)(C)CC(C)(C)C)CC2)c(Br)cn1
Reaction #1120
2-Ethyl-4-[cis-4-(1,1,3,3-tetramethylbutyl)cyclohexylamino]-5-bromopyridine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(=O)C=C([O-])c1c(OC)cccc1OC.[Na+]
Reaction #1177
expected product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #2243
oil
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(OC)c1NC(=O)CNC(=O)OC(C)(C)C
Reaction #3019
N-tert-butyloxycarbonyl-[(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylamine
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nnc(-c2ccc(OC)cc2)n1-c1ccc(OC)cc1.Cl
Reaction #4690
3,4-bis-(4-methoxyphenyl)-5-ethyl-4H-1,2,4-triazole hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nnc(-c2ccc(OC)cc2)n1-c1ccccc1.Cl
Reaction #4691
3-ethyl-5-(4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2CCNC2)cc1.Cl
Reaction #5185
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(CCN2CCCC2)=NC=C1OCc1ccccc1
Reaction #5610
5-benzyloxy-2-[2-(1-pyrrolidinyl)ethyl]4-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1cnc(C(=O)Cl)cc1OC(C)=O.Cl
Reaction #5616
4,5-diacetoxy-2-pyridinecarbonyl chloride hydrochloride
Rendimiento 158.5%DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)N[C@@H]1C(=O)N2C(C(=O)[O-])=C(C[N+]3(C)CCN(C(=O)c4cc(O)c(O)cn4)CC3)CS[C@H]12)c1nsc(N)n1
Reaction #5626
7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetamido]-3-[1-methyl-4-(4,5-dihydroxy-2-pyridylcarbonyl)-1-piperazinio]methyl-3-cephem-4-carboxylate
Rendimiento 3.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CC1OC
Reaction #6393
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CCC1O
Reaction #6394
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC(C)C)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #6395
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(Oc4cccc(C=O)c4)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #6401
title compound
Rendimiento 31.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nc(CO)n(Cc2ccncc2)c1Sc1cc(Cl)cc(Cl)c1
Reaction #8507
compound ( 12 )
DOI: 10.6084/m9.figshare.5104873.v1
N=C(NCC(=O)N[C@H]1CCNC1)NC(=O)OCc1ccc([N+](=O)[O-])cc1.O=S(=O)(O)OS(=O)(=O)O
Reaction #10041
title compound
Rendimiento 95.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=CC(=O)c1cncnc1
Reaction #42044
objective compound
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1.O=C(O)C(O)C(O)C(=O)O
Reaction #43885
oseltamivir tartrate
Rendimiento 97.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1.O=P(O)(O)O
Reaction #43886
oseltamivir phosphate
Rendimiento 56.3%DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)CCNCC1.Cl
Reaction #49263
4,4-dimethoxypiperidine hydrochloride
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1
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