dihydro-2H-pyran-4(3H)-one

CC(C)(C)OC(=O)NN=C1CCOCC1
Reaction #41159
N′-(tetrahydro-pyran-4-ylidene)-hydrazinecarboxylic acid tert-butyl ester
수율 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#CC1OC12CCOCC2
Reaction #48663
desired compound
수율 59.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
OC1(C#CCOC2CCCCO2)CCOCC1
Reaction #50176
4-hydroxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran
수율 88.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
OCC1COC2(CCOCC2)OC1
Reaction #59886
title compound
수율 64.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCN(c1c(OC)nn2c(-c3c(OC)cc(OCC)cc3OC)csc12)C1CCOCC1
Reaction #69557
title compound
수율 59.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1cccc2nc(N3CC[C@H](NC(=O)c4nc(Cl)c(CC)[nH]4)[C@H](NC4CCOCC4)C3)sc12
Reaction #71829
title compound
수율 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])CC1(O)CCOCC1
Reaction #72993
4-(nitromethyl)tetrahydro-2H-pyran-4-ol
수율 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOCc1nc2cnc3ccccc3c2n1CC1(N)CCOCC1
Reaction #73060
4-[(2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]tetrahydropyran-4-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cl.O=S(=O)(c1ccccc1)n1ccc2c(OCCNC3CCOCC3)cccc21
Reaction #78272
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
OC1(c2ccc(OCc3ccccc3)cc2)CCOCC1
Reaction #79367
4-(4-benzyloxyphenyl)tetrahydro-2H-pyran-4-ol
수율 55.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCc1nc2cnc3ccccc3c2n1CCCCNC1CCOCC1
Reaction #90307
N-[4-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]tetrahydro-2H-pyran-4-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cc(C=C2COCC(=Cc3cc(OC)c(OC)c(OC)c3)C2=O)cc(OC)c1OC
Reaction #93950
Tetrahydro-3,5-bis[(3,4,5-trimethoxyphenyl)methylene]-4H-pyran-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
COc1ccc(C=C2COCC(=Cc3ccc(OC)c(C)c3C)C2=O)c(C)c1C
Reaction #93952
yellow crystals
수율 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
COc1cc(C)c(C=C2COCC(=Cc3cc(C)c(OC)cc3C)C2=O)cc1C
Reaction #93954
yellow solid
수율 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
COc1cc(-n2ccc3cc(OC[C@@H]4CCCO4)ccc3c2=O)ccc1N1CCCN(C2CCOCC2)CC1
Reaction #156700
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CCC1COCCC1=O
Reaction #160815
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C(C#N)=C1CCOCC1
Reaction #163395
methyl 2-cyano-2-(oxan-4-ylidene)acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1nc2c(s1)COCC2
Reaction #165661
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1nc2c(s1)COCC2
Reaction #165712
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)NC(C(=O)OC)=C1CCOCC1
Reaction #167156
methoxycarbonylamino-(tetrahydropyran-4-ylidene)-acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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