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468821

Cc1cc2cccc(F)c2[nH]1
Reaction #46780
expected compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2cc(C)[nH]c12
Reaction #46782
expected compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@](O)(CC)C(=O)O[C@@H]1C[C@H](C)CC[C@H]1C(C)(C)c1ccccc1
Reaction #58772
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)[C@H](CC1CCCCC1)NC(=O)OC(C)(C)C
Reaction #87111
(S)-tert-butyl (1-cyclohexyl-4-methyl-3-oxopent-4-en-2-yl)carbamate
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)[C@H](CC1=CCCC1)NC(=O)OC(C)(C)C
Reaction #87124
(S)-tert-butyl (1-(cyclopent-1-en-1-yl)-4-methyl-3-oxopent-4-en-2-yl)carbamate
Ausbeute 52.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C1(O)CCN(C(=O)OC(C)(C)C)C1
Reaction #393754
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)NC(c1cncc(-c2ccc(C#N)c(Cl)c2)c1)C(C)C
Reaction #478469
solid
Ausbeute 23.8%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(O)c1cc(OCc2ccccc2)ccc1[N+](=O)[O-]
Reaction #483305
1-[5-(benzyloxy)-2-nitrophenyl]-2-methyl-2-propen-1-ol
Ausbeute 48.7%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C1CCC(CC)(CC(=O)OC)C(=O)C1
Reaction #570316
colorless oil
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H](CO[Si](C)(C)C(C)(C)C)N(CC(=O)C(=C)C)C(=O)OC(C)(C)C
Reaction #714254
desired product
Ausbeute 89.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2cccc(Cl)c2[nH]1
Reaction #809580
2-Methyl-7-chloro-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2cccc(Br)c2[nH]1
Reaction #809581
7-Bromo-2-methyl-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2ccc(Cl)c(Cl)c2[nH]1
Reaction #809582
6,7-Dichloro-2-methyl-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1ccc(-c2nn3c(NCCCC)cccc3c2-c2ccnc(NCCCC)n2)cc1
Reaction #948302
N-butyl-3-[2-(butylamino)-4-pyrimidinyl]-2-(4-isopropenylphenyl)pyrazolo[1,5-a]pyridin-7-amine
Ausbeute 27.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(O)c1cc(Br)ccc1F
Reaction #966769
1-(5-bromo-2-fluorophenyl)-2-methylprop-2-en-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2cccc(Cl)c2[nH]1
Reaction #977416
expected compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc2cc(C)[nH]c12
Reaction #977418
expected compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2cccc(Br)c2[nH]1
Reaction #977419
expected compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2ccc(Cl)c(Cl)c2[nH]1
Reaction #977420
expected compound
DOI: 10.6084/m9.figshare.5104873.v1
CC#CC(C)(O)CCC=C(C)C
Reaction #1013593
product
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
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