succinic acid anhydride

CCCCCCCCN(CC(O)CN(CCS(=O)(=O)O)CC(O)CN(CCCCCCCC)C(=O)CCC(=O)O)C(=O)CCC(=O)O
Reaction #1363
6,10-dihydroxy-4,12-dioctyl-3,13-dioxo-8-sulfoethyl-4,8,12-triaza-1,15-pentadecanedicarboxylic acid
Ausbeute 80.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #1597
3(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #1664
3-(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(CC(=O)OCc1ccccc1)C(=O)CCC(=O)O
Reaction #1812
title compound
Ausbeute 86.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #2169
3-(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #2210
3-(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NC(CC(=O)c1ccc(N2CCN(c3ccncc3)CC2)cc1)C(=O)O
Reaction #2336
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1ccc(C(=O)CCC(=O)O)cc1
Reaction #2982
4-OXO-4-(4-ETHYLPHENYL)BUTYRIC ACID
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CC=C1c2ccc(O)cc2Oc2cc(O)ccc21
Reaction #4977
powder
Ausbeute 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1cc2c(cc1O)Oc1cc(O)c(C)cc1C2=CCC(=O)O
Reaction #4979
powder
Ausbeute 74.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
—
Reaction #7149
di-isopropanolamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)COc1ccc(C(=O)CCC(=O)O)cc1Cl
Reaction #11413
9
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ncc(Cl)cc1NC(=O)CCC(=O)O
Reaction #11771
title compound
Ausbeute 31.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCc1cccc(C2(NC[C@@H](O)[C@H](Cc3cc(F)cc(F)c3)NC(=O)CCC(=O)O)CC2)c1
Reaction #42607
4-[((1S,2R)-1-(3,5-difluorobenzyl)-3-{[1-(3-ethylphenyl)cyclopropyl]amino}-2-hydroxypropyl)amino]-4-oxobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)CCC(=O)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1
Reaction #44932
succinylsulfathiazole
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc([C@@H]2c3cc4c(cc3[C@H](OC(=O)CCC(=O)O)[C@H]3COC(=O)[C@H]23)OCO4)cc(OC)c1OC
Reaction #44940
succinylpodophyllotoxin
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCC1CCC2C3CC=C4CC(OC(=O)NCCCCCC(=O)N5CC(OC(=O)CCC(=O)O)CC5C(OC(c5ccc(OC)cc5)c5ccc(OC)cc5)c5ccccc5)CCC4(C)C3CCC12C
Reaction #49173
compound 8
Ausbeute 89.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCCCCCCCCCCOCC(COC(=O)NCCCCCC(=O)N1CC(OC(=O)CCC(=O)O)CC1C(OC(c1ccc(OC)cc1)c1ccc(OC)cc1)c1ccccc1)OCCCCCCCCCCCCCCCCCC
Reaction #49174
compound 14
Ausbeute 47.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCCCCCCCCC1(C)CCc2c(C)c(OCCOC(=O)NCCCCCC(=O)N3CC(OC(=O)CCC(=O)O)CC3C(OC(c3ccc(OC)cc3)c3ccc(OC)cc3)c3ccccc3)c(C)c(C)c2O1
Reaction #49177
compound 21
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(C(OC(c2ccccc2)C2CN(C(=O)CCCCCNC(=O)OC3CCC4(C)C(=CCC5C4CCC4(C)C(C(C)CCCC(C)C)CCC54)C3)CC2OC(=O)CCC(=O)O)c2ccc(OC)cc2)cc1
Reaction #49195
compound 68
Ausbeute 91.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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