4-hydroxy-2-cyclopentenone

CC(C)(C)[Si](C)(C)OC1C=CC(=O)C1
Reaction #2634
title compound
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1C=CC(OC2CCCCO2)C1
Reaction #2641
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC1C=CC(=O)C1
Reaction #2643
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1C=CC(OC(c2ccccc2)(c2ccccc2)c2ccccc2)C1
Reaction #2659
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1C=CC(OC2CCCCO2)C1
Reaction #319411
4-(2-tetrahydropyranyl)oxy-2-cyclopentenone
Ausbeute 93.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CCCCC1(O)C=CC(O)C1
Reaction #1073509
4-butylcyclopent-2-ene-1,4-diol
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_12
CCCCC1(O)C=CC(O)C1
Reaction #1216180
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
COC(=O)CCC#CCCC1=CC(O)CC1=O
Reaction #1700176
4-hydroxy-2-(6-methoxycarbonyl-3-hexynyl)-2-cyclopentenone
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_03
COC(=O)CCC#CCCC1=CC(O)CC1=O
Reaction #1700180
4-hydroxy-2-(6-methoxycarbonyl-3-hexynyl)-2-cyclopentenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_03
CC(C)(C)[Si](C)(C)OC1C=CC(=O)C1
Reaction #2481062
title compound
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_09
O=C1C=CC(OC2CCCCO2)C1
Reaction #2481069
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_09
CC(C)(C)OC1C=CC(=O)C1
Reaction #2481071
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_09
O=C1C=CC(OC(c2ccccc2)(c2ccccc2)c2ccccc2)C1
Reaction #2481088
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_09