بحث البنية الفرعية

CCOC(=O)CCCCCO

COC(=O)[C@@H]1C[C@H](O)C(=O)[C@@H]2[C@@]3(C)C[C@@H](c4ccoc4)OC(=O)[C@H]3CC[C@]21C
Reaction #40591
8a
المردود 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)C(C)C)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40592
10
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40593
13
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OS(C)(=O)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40594
white solid
المردود 32.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](O[Si](C)(C)C)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40595
16
المردود 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40598
34
المردود 81.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40599
35
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)C(C)C)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40604
10
المردود 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C2CCC(O[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)CCC21
Reaction #44505
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C2CCC(O)CCC21
Reaction #44506
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCCOc1c(OC)ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc12
Reaction #48940
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCCO)OCc1ccccc1
Reaction #50193
title compound ( b )
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCCCOC(=O)c1ccccc1)OCc1ccccc1
Reaction #50194
title compound ( c )
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)CCCCCOc1ccc2nc(-c3ccccc3)n(Cc3ccccc3)c2c1
Reaction #52168
1-Benzyl-2-phenyl-6-[(5-(iso-propyl-oxycarbonyl)pentyl]oxy]-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CCC(=O)OC(C1CC=CCC1)C1CC=CCC1
Reaction #54853
di(4-cyclohexenyl)methyl succinate
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCC(O)CCCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #54880
4-(4-acetyl-8-hydroxytridec-12-en-1-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCOCC(CCCC(CCCc1ccc(C(=O)OCC)cc1)C(C)=O)OC(C)=O
Reaction #54887
Ethyl 4-(4-Acetyl-8-acetoxy-9-propoxynonyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCC(O)CCCC(CCCc1ccc(C(=O)O)cc1)C(C)=O
Reaction #75247
4-(4-acetyl-8-hydroxytridec-12-en-1-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCOCC(CCCC(CCCc1ccc(C(=O)OCC)cc1)C(C)=O)OC(C)=O
Reaction #75254
Ethyl 4-(4-Acetyl-8-acetoxy-9-propoxynonyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1C(O)CC(O)(C(=O)OCc2ccccc2)OC1C(O)C(O)COC(=O)C(NC(=O)OCc1ccccc1)C(C)C
Reaction #164435
( 1-5 )
المردود 32.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي