Teilstruktursuche

330392

Fc1ccc2c(CBr)nsc2c1
Reaction #10304
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)c2c1c(-c1ccccc1CO)cc1[nH]c3ccc(O)cc3c21
Reaction #11124
9-Hydroxy-4-[2-(hydroxymethyl)phenyl]pyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(CCC(=O)CC(C)=O)cc1
Reaction #44323
6-(4-vinylphenyl)-2,4-hexanedione
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)OC[C@H]1O[C@@H](n2cnc3c(OC)nc(N)nc32)[C@@H](O)[C@@H]1O
Reaction #49784
desired product
DOI: 10.6084/m9.figshare.5104873.v1
OC1(O)C(F)(Cl)CCCC1(Cl)Cl
Reaction #50100
diol
Ausbeute 73.9%DOI: 10.6084/m9.figshare.5104873.v1
OC1C(F)(Cl)CCCC1(Cl)Cl
Reaction #50101
alcohol
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
FC1(Cl)CCC2OC2(Cl)C1
Reaction #50102
liquid
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)CC(C)(C)c2cc(Br)ccc21
Reaction #52414
product
Ausbeute 26.4%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccccc1)N1C=C2C=COC=C3C2=C(C1)CC31OCCO1
Reaction #53612
titled compound ( 34 )
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1cc([N+](=O)[O-])ccc1OC
Reaction #56734
3-Allyloxy-4-methoxynitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)Nc1c(-c2ccc(C#Cc3ccccc3)s2)nc2c(C(=O)O)nccn12
Reaction #57386
3-(tert-butylamino)-2-(5-(phenylethynyl)thiophen-2-yl)imidazo[1,2-a]pyrazine-8-carboxylic acid
Ausbeute 44.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CC(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74961
1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-1,4-methanonaphthalene-5,8-dione
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1=CC(=O)C2C(C1=O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74963
6-tert-butyl-1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-1,4methanonaphthalene-5,8-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccccc1)c1cc(O)c2c(c1O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74964
1,2,3,4,9,9-hexachloro-1,4-dihydro-6-(phenylsulfonyl)-1,4-methanonaphthalene-5,8-diol
DOI: 10.6084/m9.figshare.5104873.v1
Oc1cc(Cl)c(O)c2c1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74966
1,2,3,4,6,9,9-heptachloro-1,4-dihydro-1,4-methanonaphthalene-5,8-diol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(O)c2c(c1O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74968
crystals
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74969
1,2,3,4,9,9-hexachloro-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(S(=O)(=O)c2ccccc2)C(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74970
1,2,3,4,9,9-hexachloro-1,4,4a,6,7,8a-hexahydro-6-phenylsulfonyl-1,4-methanonaphthalene-5,8-dione
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCSC1CC(=O)C2C(C1=O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74971
6-butylthio-1,2,3,4,9,9-hexachloro-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2OC2C(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74972
1,2,3,4,9,9-hexachloro-6,7-epoxy-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione
DOI: 10.6084/m9.figshare.5104873.v1
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