PCC

O=CCCCc1ccccc1
Reaction #974
aldehyde
Ausbeute 22.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC[C@@H]1C(=O)CC[C@@H]1CC(=O)OC
Reaction #2469
methyl (+)-(1R)-cis-3-oxo-2-pentyl-1-cyclopentaneacetate
Ausbeute 94.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4537
colorless crystals
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COCOCC(C)=CCCC(C)=CCCC(C)=CC=O
Reaction #5765
12-(methoxymethyl)oxy-3,7,11-trimethyl-2,6,10-dodecatrienal
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)c1ccc(C)c(F)c1
Reaction #8004
title compound
Ausbeute 86.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(CCc1ccccc1)COCc1ccccc1
Reaction #8285
title compound
Ausbeute 68.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCCc2cccc(COC3CCCCO3)c21
Reaction #9355
8-(tetrahydro-pyran-2-yloxymethyl)-3,4-dihydro-2H-naphthalen-1-one
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)CCCCC=O
Reaction #9897
6-oxo-hexanoic acid methyl ester
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)c1cc(CCc2cc(C=O)cc(CCc3cc(C(C)(C)C)cc(C(C)(C)C)c3)c2)cc(C(C)(C)C)c1
Reaction #47225
15
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)c1cc(CCc2cc(CCc3cc(C=O)cc(CCc4cc(CCc5cc(C(C)(C)C)cc(C(C)(C)C)c5)cc(CCc5cc(C(C)(C)C)cc(C(C)(C)C)c5)c4)c3)cc(CCc3cc(C(C)(C)C)cc(C(C)(C)C)c3)c2)cc(C(C)(C)C)c1
Reaction #47227
16
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C/C=C\COCc1ccccc1
Reaction #49831
(Z)-4-benzyloxy-2-butenal
Ausbeute 65.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
OC1(O)C(F)(Cl)CCCC1(Cl)Cl
Reaction #50100
diol
Ausbeute 73.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COC(=O)C1CC(=O)N(c2cccc(C=O)c2)C1
Reaction #51176
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
—
Reaction #54464
ketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
—
Reaction #55254
ketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCOC(=O)C(C#N)=CC1(C)CC1
Reaction #56720
ester
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1CCCc2cccc(COC3CCCCO3)c21
Reaction #56996
8-(tetrahydro-pyran-2-yloxymethyl)-3,4-dihydro-2H-naphthalen-1-one
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1(C)COC(CCC(=O)c2ccc(F)cc2)OC1
Reaction #57324
3-(5,5-dimethyl-1,3-dioxan-2-yl)-1-(4-fluorophenyl)propan-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=CC(Cc1ccc(Cl)cc1Cl)c1ccc(Cl)cc1
Reaction #58640
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@H](C)C(=O)c1ccccc1)OC)N(C)C(=O)[C@@H](NC(=O)[C@H](C(C)C)N(C)C)C(C)C
Reaction #58695
35
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
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