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CCC(C)Cc1ccccc1

CCCN(CCC)C(=O)n1cc(C)c2c1C[C@]1(c3cccc(O)c3)CCN(CC)C[C@H]1C2
Reaction #2958
(±)-trans-Dipropylaminocarbonyl-6-ethyl-8a-(3-hydroxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CC[C@@]2(c3cccc(O)c3)Cc3[nH]c(C(=O)N(C(C)C)C(C)C)c(C)c3C[C@@H]2C1.Cl
Reaction #2968
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CC[C@@]2(c3cccc(O)c3)Cc3[nH]c(C(=O)N4CCCC4)c(C)c3C[C@@H]2C1
Reaction #2974
title compound
Ausbeute 23.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)C=O
Reaction #10222
L-Rhamnose
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=NNC1c1ccccc1
Reaction #40777
desired product
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(Cc1ccc(N)cc1)(C(=O)c1ccc(F)cc1)N(C)C
Reaction #43524
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC(C)=O)CC[C@H]1C3=CC=C(OC(C)=O)[C@@]3(C)CC[C@H]21
Reaction #51638
diacetate
Ausbeute 80.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1O)CC[C@H]1C3=CC[C@H](O)[C@@]3(C)CC[C@H]21
Reaction #51639
product ( 18 )
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2CCC1CN1CCN(C(c2ccccc2)c2ccccc2)CC1
Reaction #54469
2-(4-benzhydryl-1-piperazinylmethyl)-3,4-dihydro-1(2H)-naphthalenone
DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC=CC2NC(=O)OC(=O)C12Cc1ccccc1
Reaction #64319
1-benzyl-6-methyl-isatoic anhydride
DOI: 10.6084/m9.figshare.5104873.v1
ON=C(c1ccc(F)cc1F)C1CCN(Cc2ccccc2)C1
Reaction #83909
(2,4-difluorophenyl)[1-(phenylmethyl)-3-pyrrolidinyl]methanone oxime
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2c(C3CCN(Cc4ccccc4)C3)noc2c1.O=C(O)/C=C/C(=O)O
Reaction #83910
6-fluoro-3-[1-(phenylmethyl)-3-pyrrolidinyl]-1,2-benzisoxazole fumarate
Ausbeute 74.8%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3ccc(F)cc3F)CO[C@H](CF)[C@H]2CS1
Reaction #155559
title compound
Ausbeute 104.2%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3cc(Br)c(F)cc3F)CO[C@H](CF)[C@H]2CS1
Reaction #155560
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NCc1ccc2c(c1)C(Cc1ccccc1)C(NC(=O)OC(C)(C)C)CC2
Reaction #170046
solid
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NCc1ccc2c(c1)C(Cc1ccccc1)C(N)CC2
Reaction #170050
N-((7-amino-8-benzyl-5,6,7,8-tetrahydronaphthalen-2-yl)methyl)ethanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCC2(c3cccc(O)c3)Cc3[nH]c(C(=O)N(C(C)C)C(C)C)c(C)c3CC2C1
Reaction #177380
DOI: 10.1039/C8SC04228D
COc1ccc(N2CCN(C)CC2)c2c1CCC(C(=O)Nc1ccc(N3CCOCC3)cc1)C2
Reaction #182693
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(Cc1ccccc1)C1CC(Cc2ccc(-c3ccccn3)cc2)C(=O)O1
Reaction #189376
DOI: 10.1039/C8SC04228D
COc1ccc2c(c1O)C13CCN(C)C(C2)C1CC(C)C(=O)C3
Reaction #189746
DOI: 10.1039/C8SC04228D
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