pyridinium para-toluene sulfonate

COC(=O)[C@@H]1OC(C(Cl)(Cl)Cl)N[C@H]1c1ccccc1
Reaction #1859
(4S,5R)-5-methoxycarbonyl-4-phenyl-2-trichloromethyl-1,3-oxazolidine
المردود 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(CC(OCCO)c1ccc(Cl)c(Cl)c1)C(=O)OC(C)(C)C
Reaction #1936
expected product
المردود 100.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(CCCCCOC1CCCCO1)OCC
Reaction #2109
Diethyl 5-(tetrahydropyran-2-yloxy)pentylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(OCC)C(C)(C)CCCCO
Reaction #2111
Diethyl 5-hydroxy-1,1-dimethylpentylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1C=CC(OC2CCCCO2)C1
Reaction #2641
title compound
المردود 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1ccc(OC2CCCCO2)cc1
Reaction #7427
p-tetrahydropyranyloxy benzoic acid
المردود 86.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@]12CC[C@H]3[C@@H](CC[C@@H]4CC(O)CC[C@@H]43)[C@@H]1CCC21OCCO1
Reaction #7508
title compound
المردود 94.8%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
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC1=Cc2ccccc2N(C(N)=O)c2ccccc21
Reaction #9813
10-methoxy-5H-dibenz[b,f]azepine-5-carboxamide
المردود 50.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
OCC1=NOC(CN2CCOCC2)C1
Reaction #10269
[5-((morpholin-4-yl)methyl)-4,5-dihydro-isoxazol-3-yl]methanol
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(CN1C(=O)c2cc3ccccc3cc2C1=O)C(C)=O
Reaction #10976
Methyl 2-(1,3-dioxo-1,3-dihydro-benzo[f]isoindol-2-ylmethyl)-3-oxo-butyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(CN1C(=O)c2ccc(F)cc2C1=O)C(C)=O
Reaction #10977
Methyl 2-(5-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-3-oxo-butyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(CN1C(=O)c2ccc(Cl)cc2C1=O)C(C)=O
Reaction #10978
Methyl 2-(5-chloro-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-3-oxo-butyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(CN1C(=O)c2ccc(Br)cc2C1=O)C(C)=O
Reaction #10979
Methyl 2-(5-bromo-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-3-oxo-butyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#CC1(c2ccccc2)CCCC2(C1)OCCO2
Reaction #11310
title compound
المردود 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Fc1ccc(OC2CCCCO2)c(Br)c1
Reaction #41916
2-Bromo-4-fluoro-1-(tetrahydropyran-2-yloxy)benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Br)c(OC2CCCCO2)c1
Reaction #41918
2-Bromo-5-fluoro-1-(tetrahydropyran-2-yloxy)benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1cc(OCc2ccccc2)ccn1-c1ccc(O)cc1
Reaction #43313
title compound
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1c(Br)c(Br)cnn1-c1ccc(OC2CCCCO2)cc1
Reaction #43326
title compound
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(Br)ccc1OC1CCCCO1
Reaction #43340
title compound
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
الصفحة 1التالي