tetrahydro-4H-pyran-4-ol

COC(=O)c1ccc(OC(=O)C2CCOCC2)cc1OC
Reaction #1770
methyl 4-(4-tetra-hydropyranoyloxy)-2-methoxy-benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)Nc1ccc(OC2CCOCC2)c2ccccc12
Reaction #51811
[4-(tetrahydro-pyran-4-yloxy)-naphthalen-1-yl]-carbamic acid tert-butyl ester
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C1c2ccccc2C(=O)N1OC1CCOCC1
Reaction #57440
2-(tetrahydro-2H-pyran-4-yloxy)-1H-isoindole-1,3(2H)-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1CCC(C(=O)N(c2cc(C#CC(C)(C)C)sc2C(=O)O)C2CCN(C(=O)O[C@H]3COC4OCCC43)CC2)CC1
Reaction #67572
4-[[2-carboxy-5-(3,3-dimethyl-but-1-ynyl)-thiophen-3-yl]-(4-methyl-cyclohexanecarbonyl)-amino]-piperidine-1-carboxylic acid hexahydro-furo[2,3-b]furan-3-(R)-yl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1ccc(OC2CCOCC2)nc1
Reaction #85825
white solid
Выход 79.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1(C)c2cc(OC3CCOCC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #89975
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#Cc1c(-c2ccc(OC3CCOCC3)cc2)nn2c1NCCC2c1ccccc1N
Reaction #92564
7-(2-aminophenyl)-2-(4-(tetrahydro-2H-pyran-4-yloxy)phenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrile
Выход 12.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1nc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(OC3CCOCC3)c(Cl)c2)ccc1C1CC1
Reaction #157813
(5R)-5-[(E)-2-[3-chloro-4-(tetrahydro-2H-pyran-4-yloxy)phenyl]-2-(5-cyclopropyl-6-methoxypyridin-2-yl)ethenyl]pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CS(=O)(=O)OC1CCOCC1
Reaction #174449
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(=NOC1CCOCC1)C(C)=O
Reaction #179120
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C1=Cc2cc(OC3CCOCC3)ccc2CCC1
Reaction #187289
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCc2cc(OC3CCOCC3)ccc21
Reaction #189206
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccc(F)cc1OC1CCOCC1
Reaction #190010
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Cl)OC1CCOCC1
Reaction #200476
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(OC2CCOCC2)ncc1Br
Reaction #204825
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1cccnc1OC1CCOCC1
Reaction #207230
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Oc1ccc([N+](=O)[O-])cc1)OC1CCOCC1
Reaction #219305
4-nitrophenyl tetrahydropyran-4-yl carbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Cc1ccc(S(=O)(=O)OC2CCOCC2)cc1
Reaction #227456
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Brc1ccc(COC2CCOCC2)cc1
Reaction #236823
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1c(N)cccc1OC1CCOCC1
Reaction #242860
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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