n-heptane ethyl acetate

CS(=O)(=O)OCC1CCN(C(=N)NC(=O)OCc2ccccc2)C1
Reaction #959
title compound
المردود 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)Oc1ccc2nc(C(=O)O)c(OCc3ccccc3)cc2c1
Reaction #1840
oily product
المردود 129.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)Cc1cccc(-c2ccccc2)c1
Reaction #59365
biphenyl-3-yl acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1CC(c2ccccc2Cl)Oc2ccc(O)cc21
Reaction #59563
2-(2-Chlorophenyl)-6-hydroxychroman-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CS(=O)(=O)Nc1ccc(Oc2ccc3c(c2)CCC(c2ccc(F)cc2)O3)nc1
Reaction #59573
N-{6-[2-(4-Fluorophenyl)chroman-6-yloxy]pyridin-3-yl}methane sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)CS(=O)(=O)c1ccc(C)cc1
Reaction #60674
title product
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(S(=O)(=O)OC2CCOC2)cc1
Reaction #69509
title compound
المردود 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(C)COS(=O)(=O)c1ccc(C)cc1
Reaction #69512
title compound
المردود 71.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1CC(COCc2ccccc2)C1
Reaction #69514
title compound
المردود 50.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(F)(F)CCCOS(C)(=O)=O
Reaction #69515
title compound
المردود 92.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1cc(Cl)c(N)c(OC)c1
Reaction #69517
title compound
المردود 75.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1cc(Cl)c(I)c(OC)c1
Reaction #69518
title compound
المردود 66.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc(CCl)cc(OC)c1Br
Reaction #69521
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc(COC2CCC2)cc(OC)c1Br
Reaction #69522
title compound
المردود 85.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1nn2c(Br)csc2c1NC(=O)OC(C)(C)C
Reaction #69540
title compound
المردود 66.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCc1cc(OC)c(C(=O)CBr)c(OC)c1
Reaction #69548
title compound
المردود 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCc1cc(OC)c(-c2c(OC)sc3c(NC(=O)OC(C)(C)C)c(OC)nn23)c(OC)c1
Reaction #69551
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCc1sc2c(NC(=O)OC(C)(C)C)c(COC)nn2c1-c1c(OC)cc(COC)cc1OC
Reaction #69552
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCc1cc(OC)c(-c2csc3c(NC(=O)C4(O)CC4)c(OC)nn23)c(OC)c1
Reaction #69553
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCc1cc(OC)c(-c2csc3c(NCC4(O)CC4)c(OC)nn23)c(OC)c1
Reaction #69554
title compound
المردود 60.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
الصفحة 1التالي