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470159

COC(=O)c1ccc2c(c1)c(C)c([Si](C)(C)C)n2C1CCCC1
Reaction #11513
white crystals
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)c(C)c(-c1ccccn1)n2C1CCCC1
Reaction #11514
Methyl 1-cyclopentyl-3-methyl-2-(2-pyridyl)indole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2c(c1)c1c(n2C2CCCCC2)-c2ccc(Cl)cc2N(CC(=O)N2CCCCC2)C(=O)C1
Reaction #175197
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc2c(c1)c1c(n2C2CCCCC2)-c2ccc(Cl)cc2N(CCN2CCCCC2)CC1
Reaction #230684
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc2c(ccn2C(C)C)c1
Reaction #302467
DOI: 10.1039/C8SC04228D
CC(C)n1ccc2cc(C(=O)O)ccc21
Reaction #652156
1-isopropyl-5-indole-carboxylic acid
Ausbeute 109.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(ccn2C(C)C)c1
Reaction #652157
methyl 1-isopropyl-5-indolecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2c(c1)c1c(n2C2CCCCC2)-c2ccc(Cl)cc2NC(=O)C1
Reaction #1099463
ethyl 3-chloro-12-cyclohexyl-6-oxo-5,6,7,12-tetrahydrobenzo[2,3]azepino[4,5-b]indole-9-carboxylate
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2c(c1)c1c(n2C2CCCCC2)-c2ccc(Cl)cc2N(CC(=O)N2CCCCC2)C(=O)C1
Reaction #1099464
ethyl 3-chloro-12-cyclohexyl-6-oxo-5-[2-oxo-2-(piperidin-1-yl)ethyl]-5,6,7,12-tetrahydrobenzo[2,3]azepino[4,5-b]indole-9-carboxylate
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2c(c1)c1c(n2C2CCCCC2)-c2ccc(Cl)cc2N(CCN2CCCCC2)CC1
Reaction #1099465
ethyl 3-chloro-12-cyclohexyl-5-[2-(piperidin-1-yl)ethyl]-5,6,7,12-tetrahydrobenzo[2,3]azepino[4,5-b]indole-9-carboxylate
Ausbeute 61.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc2c(c1)c1c(n2C2CCCCC2)-c2ccc(Cl)cc2N(CCN2CCCCC2)CC1
Reaction #1099466
3-chloro-12-cyclohexyl-5-[2-(piperidin-1-yl)ethyl]-5,6,7,12-tetrahydro-benzo[2,3]azepino[4,5-b]indole-9-carboxylic acid
Ausbeute 72.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1ccc2cc(C(=O)O)ccc21
Reaction #1154944
1-isopropyl-5-indole-carboxylic acid
Ausbeute 109.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(ccn2C(C)C)c1
Reaction #1154945
Methyl 1-isopropyl-5-indolecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)c(C)c([Si](C)(C)C)n2C1CCCC1
Reaction #1261820
white crystals
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)c(C)c(-c1ccccn1)n2C1CCCC1
Reaction #1261821
Methyl 1-cyclopentyl-3-methyl-2-(2-pyridyl)indole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1ccc2cc(C(=O)O)ccc21
Reaction #1649014
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc2c(c1)cc(-c1ccc(OCc3cc(OC)ccc3-c3ccc(Cl)cc3)cc1)n2C1CCCCC1
Reaction #1922771
title compound
Ausbeute 167.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1ccc2c(c1)c(C)c(C)n2C(C)c1cccc(O[C@@H](C)C(=O)OC)c1
Reaction #2257885
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1ccc2c(c1)c(C)c(C)n2C(C)c1ccc(O)cc1
Reaction #2257893
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1ccc2c(c1)c(C)c(C)n2C(C)c1ccc(O[C@@H](C)C(=O)OC)cc1
Reaction #2257894
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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