Teilstruktursuche

106444

C=C1CCC(CO)CC1
Reaction #43566
(4-methylene-cyclohexyl)-methanol
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCC(C(=O)OCC)(C(=O)OCC)CC1
Reaction #268396
DOI: 10.1039/C8SC04228D
C=C1CCC(C(=O)OCC)CC1
Reaction #378970
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCC(CC(=O)OC(C)(C)C)CC1
Reaction #379588
DOI: 10.1039/C8SC04228D
C=C1CCC(C(=O)OCC)CC1
Reaction #379929
DOI: 10.1039/C8SC04228D
C=C1CCC(C(=O)OCC)CC1
Reaction #389461
DOI: 10.1039/C8SC04228D
—
Reaction #421536
oil
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCC(C(=O)CC#N)CC1
Reaction #421537
3-(4-methylenecyclohexyl)-3-oxopropanenitrile
Ausbeute 89.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(=CC(=O)OC(C)(C)C)CC1
Reaction #497210
product
Ausbeute 62.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(=CC(=O)O)CC1
Reaction #497211
product
Ausbeute 134.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(CC(=O)O)CC1
Reaction #497212
product
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(=C2CC3C(/C=C/C(O)C4CCCCC4)CCC3C2=O)CC1
Reaction #549957
(E)-6-(3-cyclohexyl-3-hydroxyprop-1-enyl)-3-(4-ethoxycarbonylcyclohexylidene)bicyclo[3,3,0]octan-2-one
Ausbeute 73.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C1C(=O)[C@H]2[C@H](C(=O)OC(C)(C)C)[C@H]2[C@]1(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #557089
title compound
Ausbeute 97.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C1C(=O)[C@H]2[C@H](C(=O)OC(C)(C)C)[C@H]2[C@]1(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #557090
title compound
Ausbeute 98.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@]1(C(=O)OC(C)(C)C)[C@@H]2[C@@H](C(=O)OC(C)(C)C)[C@@H]2C(=O)[C@H]1CSc1ccc(F)c(F)c1
Reaction #557091
di-tert-butyl (1S,2R,3S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-{[(3,4-difluorophenyl)sulfanyl]methyl}-4-oxobicyclo[3.1.0]hexane-2,6-dicarboxylate
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SC[C@@H]2[C@H](O)[C@H]3[C@H](C(=O)OC(C)(C)C)[C@H]3[C@]2(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)ccc1F
Reaction #557093
title compound
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C1C(=O)[C@H]2[C@H](C(=O)OC(C)(C)C)[C@H]2[C@]1(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #557101
title compound
Ausbeute 91.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C1C(=O)[C@H]2[C@H](C(=O)OC(C)(C)C)[C@H]2[C@]1(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #557102
title compound
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@]1(C(=O)OC(C)(C)C)[C@@H]2[C@@H](C(=O)OC(C)(C)C)[C@@H]2C(=O)[C@H]1CSc1ccc(F)c(F)c1
Reaction #557103
title compound
Ausbeute 141.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC[C@H](C(=O)OC(C)(C)C)[C@@H](C(=O)OCc2ccccc2)C1
Reaction #560970
(1S,2S)-1-tert-butyl 2-benzyl 4-methylenecyclohexane-1,2-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter