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1079732

CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OCc4cccc(CO[Si](C)(C)C(C)(C)C)c4)C(OC)C3)C(C)C(O[Si](C)(C)C(C)(C)C)CC1=O)C(C)CC2OC
Reaction #6392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC)C3)C(C)C(O[Si](C)(C)C(C)(C)C)CC1=O)C(C)CC2OC
Reaction #6398
title compound
Ausbeute 58.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O[Si](C)(C)C(C)(C)C)C2C)C(OC)CC3C)CC1OC
Reaction #6399
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(Oc4cccc(C=O)c4)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #6401
title compound
Ausbeute 31.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCCCC1C(=O)O)N1CC[C@H](NS(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7406
title compound
Ausbeute 21.9%DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8955
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCCCN2C(=O)N1c1c(F)cc(Cl)c2nc(Cl)sc12
Reaction #50004
N-(2,4-dichloro-6-fluorobenzothiazol-7-yl)-perhydroimidazo[1,5-a]pyridine-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCN1C(=O)c1cc2ncnc(NC(C)c3nc4cc(Cl)ccc4[nH]3)c2cc1Cl
Reaction #62455
6-chloro-4-[(1R/S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-[(2R/S)-2-ethoxycarbonyl-piperidin-1-yl-carbonyl]-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCN1C(=O)c1cc2ncnc(NC(C)c3nc4cc(Cl)ccc4[nH]3)c2cc1Cl
Reaction #62490
6-chloro-4-[(1R/S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-[(2R/S)-2-ethoxycarbonyl-piperidin-1-yl-carbonyl]-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)[C@H]2CCCCN2c2nc(Cl)ncc21
Reaction #73085
Intermediate D
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1(O)CN2CCC1CC2
Reaction #76781
tan crystalline subtitle compound
Ausbeute 48.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1(O)CN2CCC1CC2
Reaction #77878
tan crystalline subtitle compound
Ausbeute 48.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@]12C[C@@H](OCc3ccc(Br)cc3)CN1C(=O)N(c1cc(Cl)cc(Cl)c1)C2=O
Reaction #78264
above-titled compound
Ausbeute 4.8%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OC(=O)c4ccccc4)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #83377
17-allyl-12-[2-(4-benzoyloxy-3-methoxycyclohexyl)-1-methyvinyl]-1,14-dihydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone
DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)CCC(CO)N(C(=O)c2ccccc2-c2ccccc2)C1
Reaction #89089
biphenyl-2-yl(2-(hydroxymethyl)-5,5-dimethoxypiperidin-1-yl)methanone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC1(OCC)CCC(CO)NC1
Reaction #89107
rac-(5,5-diethoxypiperidin-2-yl)methanol
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1C2CCCCC2CN1C(=O)c1sc(C)nc1-c1ccccc1
Reaction #89114
Ethyl 2-(2-(2-methyl-4-phenylthiazole-5-carbonyl)octahydro-1H-isoindol-1-yl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1C2CCCCC2CN1C(=O)c1ccccc1-c1ccccc1
Reaction #89115
Ethyl 2-(2-(biphenylcarbonyl)octahydro-1H-isoindol-1-yl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1C2CCCCC2CN1C(=O)c1nc(C)sc1-c1ccccc1
Reaction #89116
Ethyl 2-(2-(2-methyl-5-phenylthiazole-4-carbonyl)octahydro-1H-isoindol-1-yl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(=O)CCN1[C@@H](C)c1ccccc1
Reaction #89424
title compound
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1
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