部分構造検索

C1CC(C1)Br

COC(=O)C1CC(Br)C1C(=O)OC
Reaction #6070
title compound
収率 19.5%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(OC2CCC2)cc1
Reaction #7472
4-cyclobutyloxybenzaldehyde
収率 75.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#Cc2cn(C3CCC3)c(C)n2)ccn1
Reaction #8974
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(CC1CCC1)c1cccc(C#N)c1
Reaction #58666
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC3CCC3)cc2n1Cc1cccnc1
Reaction #68421
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC23CC4CC(CC2C4)C3)SC12CCC2
Reaction #74320
6-(tricyclo[3.3.1.0˜3,7˜]non-3-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2CCCCCCC2)SC12CCC2
Reaction #74322
6-(Cyclooctylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2CCCCCC2)SC12CCC2
Reaction #74323
6-(Cycloheptylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2CC3CCC2C3)SC12CCC2
Reaction #74324
6-(Bicyclo[2.2.1]hept-2-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(NC2=NC(=O)C3(CCC3)S2)C1(C)C
Reaction #74325
6-[(2,2,3,3-Tetramethylcyclopropyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1NC1=NC(=O)C2(CCC2)S1
Reaction #74326
6-[(2-Methylphenyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N=C(NC2(c3ccc(Cl)cc3)CCC2)SC12CCC2
Reaction #74353
6-{[1-(4-Chlorophenyl)cyclobutyl]amino}-5-thia-7-azaspiro[3.4]oct-6-en-8-one
DOI: 10.6084/m9.figshare.5104873.v1
c1cc(N2CCCNCC2)nc(-n2ncc3cnc(-c4cnn(C5CCC5)c4)cc32)c1
Reaction #86127
solid
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccnc1SC1CCC1
Reaction #91144
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc(SC2CCC2)n1
Reaction #91161
title compound
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C)n(-c2ccc(OC3CCC3)c(F)c2)c(=O)c1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #179004
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(CC2CCCCC2)C(C(O)C2CCC2)OC1(C)C
Reaction #183708
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(NC(=O)c2cc(Cl)cc(Cl)c2OC2CCC2)Cc2ccc(F)cc2C1
Reaction #184611
DOI: 10.1039/C8SC04228D
O=S(=O)(c1cccc2ccccc12)C1CCC1
Reaction #186324
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(C(=O)C(CCC(=O)OC(C)(C)C)NC(=O)c2cc(OC3(C(=O)OCC)CCC3)n(-c3ccccc3)n2)CC1
Reaction #205004
DOI: 10.1039/C8SC04228D
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