Substructure Search

COCCCl

CC(C)(C)OCC(Cl)CN1CCCC1
Reaction #4604
oily title compound
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
c1ncc2cn[nH]c2n1
Reaction #53248
pyrazolo[3,4-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Cl)c(Cl)nc1Cl
Reaction #81577
2,3,5,6-tetrachloropyridine
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(=O)Cl
Reaction #84024
t-butyl 2-chloro-2-oxoacetate
Yield 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
Yield 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
Yield 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
CN(C)CCOc1ccccc1C=Cc1nc2ccccc2n1C
Reaction #94401
2-[o-(β-Dimethylamino-ethoxy)-styryl]-1-methyl-benzimidazole
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
Yield 79.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(OC)C(=O)Nc1cc(Cl)cc(Cl)c1
Reaction #175736
DOI: 10.1039/C8SC04228D
CC#CCOc1cc(OCC(C)(Cl)Cl)ncn1
Reaction #176361
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=NOC)C1(CCl)OCCO1
Reaction #176494
DOI: 10.1039/C8SC04228D
CC(=O)C(=NOCC(=O)OCC(Cl)(Cl)Cl)C(=O)OC(C)(C)C
Reaction #183281
DOI: 10.1039/C8SC04228D
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