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ClC(Cl)(Cl)Cl.O

C[C@@H]1C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)C1=O
Reaction #2977
product
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(C[C@H](N=C=S)c2csc(-c3ccccc3)n2)cc1
Reaction #88332
desired product
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=S)N[C@@H](Cc1ccc([N+](=O)[O-])cc1)c1csc(-c2cccs2)n1
Reaction #88334
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1CBr
Reaction #348483
o-nitrobenzyl bromide
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@]1(C(C)(C)O)C=C[C@@H](NC(=O)OC(C)(C)C)C1
Reaction #357774
desired product
Ausbeute 22.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC[C@H](NP(=O)(Cc1ccccc1)Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)O
Reaction #367957
dibenzylphosphoryl-L-glutamyl-L-prolyl-L-proline
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(C[C@H](N=C=S)c2csc(-c3ccccc3)n2)cc1
Reaction #422218
desired product
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=S)N[C@@H](Cc1ccc([N+](=O)[O-])cc1)c1csc(-c2cccs2)n1
Reaction #422220
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)c1cc2cc(O)c(Cl)c(Cl)c2s1
Reaction #458171
6,7-dichloro-5-hydroxy-α,α-dimethylbenzo[b]thiophene-2-methanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)c1cc2cc(O)c(Cl)c(Cl)c2s1
Reaction #458190
6,7-dichloro-5-hydroxy-α-methylbenzo[b]thiophene-2-methanol
DOI: 10.6084/m9.figshare.5104873.v1
CCOCn1c(CO)nc2c(N(Cc3ccccc3)Cc3ccccc3)nc3ccccc3c21
Reaction #462168
4-bis(phenylmethyl)amino-1-ethoxymethyl-1H-imidazo[4,5-c]quinolin-2-methanol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCO/N=[N+](\[O-])N1CCC[C@H]1C(=O)O
Reaction #475395
title product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2cc(C#N)c(C(F)(F)F)n2)cc1.c1coc(-c2ccn[nH]2)c1
Reaction #481995
title compound
Ausbeute 102.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C(F)(F)F)nn(-c2ccc(OC)cc2)c1C(=O)O
Reaction #481998
title compound
Ausbeute 53.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(C[C@H](N=C=S)c2csc(-c3ccccc3)n2)cc1
Reaction #512075
desired product
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=S)N[C@@H](Cc1ccc([N+](=O)[O-])cc1)c1csc(-c2cccs2)n1
Reaction #512077
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1Cc2cccnc2N(c2cccc(F)c2)C1=O
Reaction #523590
1-(m-fluorophenyl)-3-methyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine
Ausbeute 50.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCN(CC)CCC(O)c1ccc(NS(C)(=O)=O)cc1
Reaction #553552
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)O)C(F)(F)F
Reaction #560543
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(CC(=O)O)C[C@@H](C(=O)Nc2ccccc2)n2c1ncc(N(Cc1cccc(C(F)(F)F)c1)C(=O)OCc1ccccc1)c2=O
Reaction #568438
117b
DOI: 10.6084/m9.figshare.5104873.v1
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