DEAD

O=C(OCc1ccccc1)N1CCC(N2C(=O)c3ccccc3C2=O)CC1
Reaction #1173
1-benzyloxycarbonyl-4-phthalimidylpiperidine
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1c(F)nc(F)c(F)c1OC(C)(C)C
Reaction #1971
title product
Выход 85.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)[C@H](C)Oc1ccccc1C=Cc1cc2ccccc2n1C
Reaction #2244
(S)-2-{2[2-(1-methoxycarbonylethoxy)phenyl]vinyl}-1-methylindole
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)COc1ccc(OC2CCN(c3ccncc3)CC2)cc1
Reaction #2322
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(-c2nnn[nH]2)cc1Br
Reaction #3074
5-(3'-bromo-4'-methylphenyl)tetrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #5043
compound
Выход 71.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1ccccc1-c1cn2c(n1)C(CCSC(c1ccccc1)(c1ccccc1)c1ccccc1)N(C(=O)OC(C)(C)C)CC2
Reaction #6869
foam
Выход 111.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Ic1ccc(OCC2CC3C=CC2C3)cc1
Reaction #7424
8
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N1CCC2(CC1)CCn1nc(Cc3ccccc3)cc12
Reaction #8871
title compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N
Reaction #40927
NH3
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)[Si](C)(C)OCC1Cc2ccc3c(c2O1)CCC3
Reaction #42192
(±)-tert-butyl(dimethyl)(3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-ylmethoxy)silane
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)[Si](C)(C)OCC1Cc2ccc3c(c2O1)CCCC3
Reaction #42198
(±)-tert-butyl(2,3,6,7,8,9-hexahydronaphtho[1,2-b]furan-2-ylmethoxy)dimethylsilane
Выход 80.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(S(=O)(=O)OCC2Cc3cc(C)c4c(c3O2)CCC4)cc1
Reaction #42204
(±)-(5-methyl-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methyl 4-methylbenzenesulfonate
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc2c(c3c1C1CCC3CC1)OC(COS(=O)(=O)c1ccc(C)cc1)C2
Reaction #42216
(±)-(5-methoxy-2,3,6,7,8,9-hexahydro-6,9-ethanonaphtho[1,2-b]furan-2-yl)methyl 4-methylbenzenesulfonate
Выход 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1c2ccccc2C(=O)N1CC1Cc2ccc3c(c2O1)CCC3
Reaction #42234
(±)-2-(3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-ylmethyl)-1H-isoindole-1,3(2H)-dione
Выход 77.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C[C@H](C)SC(C)=O
Reaction #50704
title compound
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COc1cc2cc(OC3CCCCC3)cnc2cc1OC
Reaction #51615
3-Cyclohexyloxy-6,7-dimethoxyquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
c1ccc(Nc2cnc3cc(O[C@@H]4CCOC4)ccc3n2)cc1
Reaction #51620
Phenyl-[6-(tetrahydrofuran-3-(R)-yl-oxy)quinoxalin-2-yl]amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(C)OC(=O)Nc1ccc(OC2CCOCC2)c2ccccc12
Reaction #51811
[4-(tetrahydro-pyran-4-yloxy)-naphthalen-1-yl]-carbamic acid tert-butyl ester
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Clc1ccc(OCCN2CCOCC2)c(C2CCCCC2)c1
Reaction #52639
3-cyclohexyl-4-morpholinoethoxy-chlorobenzene
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
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