1,4-dioxa-spiro[4.5]decan-8-ol

Cc1c(OC2CCC3(CC2)OCCO3)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
Reaction #59914
title compound
Yield 7.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CS(=O)(=O)OC1CCC2(CC1)OCCO2
Reaction #69264
1,4-Dioxaspiro[4.5]dec-8-yl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CS(=O)(=O)OC1CCC2(CC1)OCCO2
Reaction #73295
1,4-Dioxaspiro[4.5]dec-8-yl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Clc1ncnc2c1c(I)cn2C1CCC2(CC1)OCCO2
Reaction #79844
4-chloro-7-(1,4-dioxaspiro[4.5]dec-8-yl)-5-iodo-7H-pyrrolo[2,3-d]pyrimidine
Yield 200.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
c1ccc(OC2CCC3(CC2)OCCO3)cc1
Reaction #188449
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCCCCCCOC1CCC2(CC1)OCCO2
Reaction #231314
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CS(=O)(=O)OC1CCC2(CC1)OCCO2
Reaction #236114
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSC(=S)OC1CCC2(CC1)OCCO2
Reaction #246488
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3)cc1)nn2C1CCC2(CC1)OCCO2
Reaction #262823
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCc1nc(CC)n(-c2ccc(OC3CCC4(CC3)OCCO4)cc2)c(=O)c1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #284742
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1ncnc2c1c(I)nn2C1CCC2(CC1)OCCO2
Reaction #290762
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(S(=O)(=O)OC2CCC3(CC2)OCCO3)cc1
Reaction #294123
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
BrC1CCC2(CC1)OCCO2
Reaction #297483
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1CCC2(CC1)OCCO2
Reaction #380371
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
c1ccc(COC2CCC3(CC2)OCCO3)cc1
Reaction #387855
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1ccc(S(=O)(=O)OC2CCC3(CC2)OCCO3)cc1
Reaction #445535
subtitled intermediate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_08
CS(=O)(=O)OC1CCC2(CC1)OCCO2
Reaction #476622
title compound
Yield 98.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=[N+]([O-])c1ccc(F)cc1OC1CCC2(CC1)OCCO2
Reaction #493189
8-(5-Fluoro-2-nitro-phenoxy)-1,4-dioxa-spiro[4.5]decane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3)cc1)nn2C1CCC2(CC1)OCCO2
Reaction #519322
1-(1,4-dioxaspiro[4.5]dec-8-yl)-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
Nc1ncnc2c1c(I)nn2C1CCC2(CC1)OCCO2
Reaction #519326
1-(1,4-dioxaspiro[4.5]dec-8-yl)-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-ylamine
Yield 54.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
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