Teilstruktursuche

OCCBr

CCOC(=O)C(CC)N1CC(c2ccccc2)CCC1=O
Reaction #7495
ester
Ausbeute 70.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C(Br)=N/Nc1ccccc1Cl
Reaction #7501
title compound
Ausbeute 71.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2nc3ccccc3o2)cc1OCCO[Si](C)(C)C(C)(C)C
Reaction #7813
2-[3-(2-{[tert-butyl(dimethyl)silyl]oxy}-ethoxy)-4-methylphenyl]-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CCO[Si](C)(C)C(C)(C)C)CCN(C(=O)OC(C)(C)C)CC1
Reaction #8862
tert-Butyl 4-methoxycarbonyl-4-(2-(tert-butyldimethylsilyloxy)eth-1-yl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCNc1cc(Cl)cnc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11814
title compound
Ausbeute 36.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCCOc1cccc([N+](=O)[O-])c1[N+](=O)[O-]
Reaction #46880
tert-Butyl-[2-(2,3-dinitro-phenoxy)-ethoxy]-dimethyl-silane
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC)Nc1ccc2ccccc2c1
Reaction #51328
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C#CC1CCCCC1Cl
Reaction #54843
propiolic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCC1OC(CNc2ccccc2OC)OC1C
Reaction #56319
N-(4-methyl-5-ethyl-1,3-dioxolan-2-ylmethyl)-2-methoxyaniline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(OCCO[Si](C)(C)C)c(I)cc1Oc1cnc(N)nc1N
Reaction #66679
5-[5-Iodo-2-isopropyl-4-(2-trimethylsilanyloxy-ethoxy)-phenoxy]-pyrimidine-2,4-diamine
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCCBr
Reaction #68810
liquid
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(NC(=O)c1cccc(-c2ccncc2N(CCO[Si](C)(C)C(C)(C)C)S(C)(=O)=O)c1)c1ccccc1
Reaction #72274
3-(3-(N-(2-(tert-butyldimethylsilyloxy)ethyl)methylsulfonamido) pyridin-4-yl)-N-(2-phenylpropan-2-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCC1SC(NC2CC3CCC2C3)=NC1=O
Reaction #74315
2-(bicyclo[2.2.1]hept-2-ylamino)-5-ethyl-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CCC1SC(NC2CCCCC2)=NC1=O
Reaction #74317
2-(cyclohexylamino)-5-ethyl-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #74405
solid
DOI: 10.6084/m9.figshare.5104873.v1
OC1C=CC(Cl)=CC1(O)Br
Reaction #80941
2-bromo-4-chlorocatechol
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86630
compound 5
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(C#N)cc2[C@@H](N2CCCC2=O)[C@@H]1O
Reaction #93186
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)Cc1cccc(Cl)c1Cl
Reaction #94009
methyl 2-bromo-3-(2,3-dichlorophenyl)propionate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnc3n2CCCC3(CCO)c2ccc(Cl)c(Cl)c2)ccc1-c1cnc(C)o1
Reaction #158295
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter