cyclobutanone

OC1(c2ccc(Br)cc2)CCC1
Reaction #9329
3-1
Выход 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCn1cc(C(O)C2CCN(C3CCC3)CC2)nc1-c1cccc2ccccc12
Reaction #40751
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)NN=C1CCC1
Reaction #41196
N′-cyclobutylidene-hydrazinecarboxylic acid tert-butyl ester
Выход 81.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCN(C2CCC2)CC1
Reaction #45061
tert-butyl 4-cyclobutylpiperazine-1-carboxylate
Выход 53.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCN(C2CCC2)CC1
Reaction #45102
tert-butyl 4-cyclobutylpiperazine-1-carboxylate
Выход 50.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
OC1(c2ccc(Br)cc2)CCC1
Reaction #48042
1-(4-bromophenyl)-cyclobutanol
Выход 34.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(c1cc2cc(OC3CCN(C4CCC4)CC3)ccc2[nH]1)N1CCC(F)(F)CC1
Reaction #48173
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1cc2cc(OC3CCN(C4CCC4)CC3)ccc2n1-c1cncnc1
Reaction #48175
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(OCC2COC3(CCC3)OC2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59906
title compound
Выход 6.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1(C)CC(c2ccccc2N2CCN(C3CCC3)CC2)CC(C)(C)C1
Reaction #60505
1-cyclobutyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)c1cccc2nc(N3CC[C@H](NC(=O)c4nc(Cl)c(CC)[nH]4)[C@H](NC4CCC4)C3)sc12
Reaction #71828
title compound
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])CC1(O)CCC1
Reaction #72983
1-(nitromethyl)cyclobutanol
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])CC1(O)CCC1
Reaction #73073
1-(nitromethyl)cyclobutanol
Выход 49.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(F)c2c1C[C@@H](N(C(C)C)C1CCC1)CO2
Reaction #80554
title compound
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1ccc(F)c2c1C[C@@H](N(C1CCCC1)C1CCC1)CO2
Reaction #80564
title compound
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC1(C)c2cc(N3CCN(C4CCC4)CC3)ccc2C(=O)c2c1[nH]c1nc(C#N)ccc21
Reaction #90168
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc(CN2C(=O)CCC2C=C(c2ccc(C(C)(C)C)cc2)c2ccc(C3(O)CCC3)c(OC)n2)c(OC)c1
Reaction #157856
5-{2-(4-tert-butylphenyl)-2-[5-(1-hydroxycyclobutyl)-6-methoxypyridin-2-yl]ethenyl}-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NS(=O)(=O)CC1(O)CCC1
Reaction #159537
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COCC1CN(C2CCC2)CC2(CCN(C(=O)c3ccc(OC(C)C)c(C)c3)CC2)O1
Reaction #160238
(4-cyclobutyl-2-(methoxymethyl)-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)(4-isopropoxy-3-methylphenyl)methanone
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)NN=C1CCC1
Reaction #185970
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Страница 1Далее