Recherche de Sous-structure

CCOCCCl

CC(C)(C)OCC(Cl)CN1CCCC1
Reaction #4604
oily title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(OCCOCCOCCO)c1
Reaction #5144
2-(2-(2-(3-nitrophenoxy)ethoxy)ethoxy)ethanol
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CNCCOCCOCCNCc2ccccc2)cc1
Reaction #6312
1,10-dibenzyl-4,7-dioxa-1,10-diazadecane
DOI: 10.6084/m9.figshare.5104873.v1
C=C(CC)OC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CCC1O
Reaction #6397
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
CCCOCCOc1ccc(C(=O)O)cc1
Reaction #11500
title compound
Rendement 105.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)C(=O)OC(C)(C)C)c1
Reaction #41363
tert-Butyl[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]carbamoylformate
DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Cl)c(Cl)nc1Cl
Reaction #81577
2,3,5,6-tetrachloropyridine
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc2nc(CCl)[nH]c2c1
Reaction #82263
2-chloromethyl-5-benzimidazolecarbonitrile
Rendement 54.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(=O)Cl
Reaction #84024
t-butyl 2-chloro-2-oxoacetate
Rendement 40.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(=O)Cl
Reaction #84025
Compound 34
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)C(=O)[C@H]5C[C@H]5[C@H]4[C@@H]3[C@H](Cl)[C@H]3O[C@]32C1
Reaction #93689
7α-chloro-5,6β-epoxy-15β,16β-methylene-3β-pivaloyloxy-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)C(=O)[C@H]5C[C@H]5[C@H]4[C@@H]3C=C[C@]2(O)C1
Reaction #93690
5-hydroxy-15β,16β-methylene-3β-pivaloyloxy-5β-androst-6-en-17-one
Rendement 74.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)C(=O)[C@H]5C[C@H]5[C@H]4[C@@H]3[C@H](Cl)[C@H]3O[C@]32C1
Reaction #93692
3β-(tert.-butyldimethylsilyloxy)-7α-chloro-5,6β-epoxy-15β,16β-methylene-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(C)C
Reaction #93693
diisopropyl ether
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C=C[C@]4(O)C[C@@H](O)CC[C@]34C)[C@@H]1[C@@H]1C[C@@H]1C2=O
Reaction #93694
3β,5-dihydroxy-15β,16β-methylene-5β-androst-6-en-17-one
Rendement 94.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H]([C@H](Cl)[C@H]4O[C@]45C[C@@H](O[Si](Cc4ccccc4)(Cc4ccccc4)Cc4ccccc4)CC[C@]35C)[C@@H]1[C@@H]1C[C@@H]1C2=O
Reaction #93696
3β-tribenzylsilyloxy-7α-chloro-5,6β-epoxy-15β,16β-methylene-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(C)C
Reaction #93697
diisopropyl ether
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Cl)CCCNC1=O
Reaction #158353
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2cc(F)c(F)c(F)c2)CCCNC1=O
Reaction #158354
title compound
Rendement 79.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)N(Cc1ccccc1)[C@H]1[C@H](O)CCC1(F)F
Reaction #168334
trans-N-benzyl-2-chloro-N-(2,2-difluoro-5-hydroxycyclopentyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
Page 1Suivant