Busqueda de Subestructura

CC(C)(CCCl)O

C=CC12C=C(OCOCCOC)C(OCOCCOC)=C(Cl)C1(Cl)O2
Reaction #2676
expected product
Rendimiento 99.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(C)(CCCl)Oc2ncccc2C1=O.Cl
Reaction #4915
desired product
Rendimiento 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCC1(C)CN(C)C(=O)c2cccnc2O1.Cl.Cl
Reaction #4944
white crystals
Rendimiento 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCC1(C)CN(C)C(=S)c2cccnc2O1.Cl
Reaction #4945
yellow crystals
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCSc1cccc2nccn12)c1ccccc1O
Reaction #5551
desired product
Rendimiento 56.0%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
Rendimiento 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
Rendimiento 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
C[C@]12CCC(=O)C=C1CC[C@@H]1C2=CC[C@@]2(C)[C@H]1CC[C@]2(O)C(=O)CCl
Reaction #94829
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC12C=CC(CC1)C(=O)CC2=O
Reaction #159459
1-methoxybicyclo[3.2.2]non-6-en-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
CNC1=Nc2ccccc2C(O)(c2ccccc2)C1(C)C
Reaction #180392
DOI: 10.1039/C8SC04228D
CN1C(=O)C(C)(C(=O)CCl)Oc2cc(Oc3c(F)cc(C(F)(F)F)cc3Cl)ccc21
Reaction #183277
DOI: 10.1039/C8SC04228D
C=CCC(O)(CCNC1CCCN(C(=O)OC(C)(C)C)C1)c1ccc(F)cc1
Reaction #196605
DOI: 10.1039/C8SC04228D
C=C(COC1CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CCl)c1ccccc1
Reaction #199533
DOI: 10.1039/C8SC04228D
C=CCC1(c2ccccc2)CCN(C2CC2c2ccccc2)C(=O)O1
Reaction #199749
DOI: 10.1039/C8SC04228D
CC12CCC(=O)C=C1CCC1C2CCC2(C)C1CCC2(O)C(=O)CCl
Reaction #209314
DOI: 10.1039/C8SC04228D
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