Substructure Search

151849

CC1(C)COC(C)(CCO)OC1
Reaction #59923
title compound
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCCC2(C)OCC(C)(C)CO2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59924
title compound
Yield 7.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CCO)OCC2(CC2)CO1
Reaction #59925
title compound
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCCC2(C)OCC3(CC3)CO2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59926
title compound
Yield 5.5%DOI: 10.6084/m9.figshare.5104873.v1
CC=CC1(CCO)OCC(C)(CCC)CO1
Reaction #466507
2-hydroxyethyl-5-methyl-2-(1-propenyl)-5-propyl-1,3-dioxane
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc([C@H]2C[C@]3(C)C(=O)CC[C@H]3[C@@H]3CC[C@@]4(O)CC5(CCC4=C32)OCC(C)(C)CO5)cc1
Reaction #639237
title compound
Yield 62.2%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc([C@H]2C[C@]3(C)C(=O)CC[C@H]3[C@@H]3CC[C@@]4(O)CC5(CCC4=C32)OCC(C)(C)CO5)cc1
Reaction #642407
title compound
Yield 62.2%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc([C@H]2C[C@]3(C)C(=O)CC[C@H]3[C@@H]3CC[C@@]4(O)CC5(CCC4=C32)OCC(C)(C)CO5)cc1
Reaction #687363
title compound
Yield 62.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C[C@H](c3ccc(C=O)cc3)C3=C4CCC(=O)C=C4CC[C@H]3[C@@H]1CC[C@@]2(O)C(F)(F)C(F)(F)F
Reaction #1613849
4-[(11β,17β)-17-Hydroxy-3-oxo-17-(pentafluoroethyl)estra-4,9-dien-11-yl]benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@H](NC(=O)OC(C)(C)C)C(O)c1cc1=O
Reaction #1695888
product
Yield 47.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)COC(C)(CCO)OC1
Reaction #1732771
title compound
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCCC2(C)OCC(C)(C)CO2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #1732772
title compound
Yield 7.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CCO)OCC2(CC2)CO1
Reaction #1732773
title compound
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(OCCC2(C)OCC3(CC3)CO2)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #1732774
title compound
Yield 5.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2=CC(=O)CCC2CN(C)C)c1.Cl
Reaction #2268446
4-dimethylaminomethyl-3-(3-methoxy-phenyl)-cyclohex-2-enone hydrochloride
Yield 78.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC1CCC(=O)C=C1c1cccc(O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)c1
Reaction #2268447
title compound
DOI: 10.6084/m9.figshare.5104873.v1