Recherche de Sous-structure

C1CC(=O)C1

CC(C)(C)OC(=O)NCC1CC(=O)C1
Reaction #6045
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CC(CO)C1=O)c1ccccc1
Reaction #6055
title compound
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CC(CO)C1O)c1ccccc1
Reaction #6056
title compound
Rendement 101.8%DOI: 10.6084/m9.figshare.5104873.v1
OC1(c2ccc(Br)cc2)CCC1
Reaction #9329
3-1
Rendement 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(C(O)C2CCN(C3CCC3)CC2)nc1-c1cccc2ccccc12
Reaction #40751
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NN=C1CCC1
Reaction #41196
N′-cyclobutylidene-hydrazinecarboxylic acid tert-butyl ester
Rendement 81.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2C(O)CCC12
Reaction #43463
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CCC2C(=O)CC12)c1ccccc1
Reaction #43464
title compound
Rendement 86.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2C(CCC2OC(=O)c2ccccc2)N1
Reaction #43465
1J
Rendement 133.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C2CCC2)CC1
Reaction #45061
tert-butyl 4-cyclobutylpiperazine-1-carboxylate
Rendement 53.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C2CCC2)CC1
Reaction #45102
tert-butyl 4-cyclobutylpiperazine-1-carboxylate
Rendement 50.5%DOI: 10.6084/m9.figshare.5104873.v1
OC1(c2ccc(Br)cc2)CCC1
Reaction #48042
1-(4-bromophenyl)-cyclobutanol
Rendement 34.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc2cc(OC3CCN(C4CCC4)CC3)ccc2[nH]1)N1CCC(F)(F)CC1
Reaction #48173
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(OC3CCN(C4CCC4)CC3)ccc2n1-c1cncnc1
Reaction #48175
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(O)CC(C)C1
Reaction #48328
1-Allyl-3-methylcyclobutanol
Rendement 46.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(OCc2ccccc2)C1
Reaction #48331
3-(benzyloxy)cyclobutanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CC(=O)C1(Cl)Cl
Reaction #48666
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CC(=O)C1
Reaction #48667
desired compound
Rendement 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H]1C[C@@H](O)C1
Reaction #48668
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCC2COC3(CCC3)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59906
title compound
Rendement 6.2%DOI: 10.6084/m9.figshare.5104873.v1
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