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5774

CC(C)(C)OC1C=CC(=O)C1
Reaction #2643
title compound
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCC1(O)CCc2ccccc2C12CCCC2)OCC(Cl)(Cl)Cl
Reaction #5638
title compound
Выход 78.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC(C)C)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #6395
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC(C)C)C3)C(C)CCC1=O)C(C)CC2OC
Reaction #6396
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=N)C(Cl)(Cl)Cl)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40596
21
Выход 37.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)N(C(=O)OCC(Cl)(Cl)Cl)[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H]1CC(=O)CN1C2=O
Reaction #47144
26
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccc(OCCO)cc2)C[C@@H]2CN(C(C)=O)C[C@H]1N2C(=O)OC(C)(C)C(Cl)(Cl)Cl
Reaction #61309
(rac.)-(1R*,5S*)-3-Acetyl-7-[4-(2-hydroxyethoxy)phenyl]-3,9-diazabicyclo-[3.3.1]non-6-ene-6,9-dicarboxylic acid 6-ethyl ester 9-(2,2,2-trichloro-1,1-dimethylethyl) ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC2CC(c3ccc(OCCOc4cc(F)ccc4Cl)cc3)=C(C(=O)O)C(C1)N2C(=O)OC(C)(C)C(Cl)(Cl)Cl
Reaction #61311
3-Acetyl-7-{4-[2-(2-chloro-5-fluorophenoxy)ethoxy]phenyl}-3,9-diazabicyclo-[3.3.1]non-6-ene-6,9-dicarboxylic acid 9-(2,2,2-trichloro-1,1-dimethylethyl) ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1C[C@H]2CC(c3ccc(OCCOc4cc(F)ccc4Cl)cc3)=C(C(=O)N(Cc3cccc(Cl)c3Cl)C3CC3)[C@@H](C1)N2.O=CO
Reaction #61348
(rac.)-(1R*,5S*)-3-Acetyl-7-{4-[2(2-chloro-5-fluorophenoxy)ethoxy]phenyl}-3,9-diazabicyclo[3.3.1]non-6-ene-6-carboxylic acid cyclopropyl-(2,3dichlorobenzyl)amide formate salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1C[C@H]2CC(c3ccc(OCCOc4cc(F)ccc4Cl)cc3)=C(C(=O)N(Cc3cccc(C)c3C)C3CC3)[C@@H](C1)N2.O=CO
Reaction #61349
(rac.)-(1R*,5S*)-3-Acetyl-7-{4-[2-(2-chloro-5-fluorophenoxy)ethoxy]phenyl}-3,9-diazabicyclo[3.3.1]non-6-ene-6-carboxylic acid cyclopropyl-(2,3-dimethylbenzyl)amide formate salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1C[C@H]2CC(c3ccc(OCCOc4cc(F)ccc4Cl)cc3)=C(C(=O)N(Cc3ccccc3Br)C3CC3)[C@@H](C1)N2.O=CO
Reaction #61350
(rac.)-(1R*,5S*)-3-Acetyl-7-{4-[2-(2-chloro-5-fluorophenoxy)ethoxy]phenyl}-3,9-diazabicyclo[3.3.1]non-6-ene-6-carboxylic acid (2-bromobenzyl)cyclopropylamide formate salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1C[C@H]2CC(c3ccc(OCCOc4cc(F)ccc4Cl)cc3)=C(C(=O)N(Cc3ccccc3Cl)C3CC3)[C@@H](C1)N2.O=CO
Reaction #61351
(rac.)-(1R*,5S*)-3-Acetyl-7-{4-[2-(2-chloro-5-fluorophenoxy)ethoxy]phenyl}-3,9-diazabicyclo[3.3.1]non-6-ene-6-carboxylic acid (2-chlorobenzyl)-cyclopropylamide formate salt
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)c(CN(C(=O)C2=C(c3ccc(OCCOc4cc(F)ccc4Cl)cc3)C[C@@H]3CN(C(C)=O)C[C@H]2N3)C2CC2)c1.O=CO
Reaction #61352
(rac.)-(1R*,5S*)-3-Acetyl-7-{4-[2-(2-chloro-5-fluorophenoxy)ethoxy]phenyl}-3,9-diazabicyclo[3.3.1]non-6-ene-6-carboxylic acid cyclopropyl-(2-fluoro-5-methoxybenzyl)amide formate salt
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(CN(C(=O)C2=C(c3ccc(OCCOc4cc(F)ccc4Cl)cc3)C[C@@H]3CN(C(C)=O)C[C@H]2N3)C2CC2)c1.O=CO
Reaction #61353
(rac.)-(1R*,5S*)-3-Acetyl-7-{4-[2-(2-chloro-5-fluorophenoxy)ethoxy]-phenyl}-3,9-diazabicyclo[3.3.1]non-6-ene-6-carboxylic acid cyclopropyl-(3-methoxybenzyl)amide formate salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1C[C@H]2CC(c3ccc(OCCOc4cc(F)ccc4Cl)cc3)=C(C(=O)N(Cc3cc4c(cc3Cl)OCO4)C3CC3)[C@@H](C1)N2.O=CO
Reaction #61354
(rac.)-(1R*,5S*)-3-Acetyl-7-{4-[2-(2-chloro-5-fluorophenoxy)ethoxy]phenyl}-3,9-diazabicyclo[3.3.1]non-6-ene-6-carboxylic acid (6-chlorobenzo[1,3]-dioxol-5-ylmethyl)cyclopropylamide formate salt
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CN(C(=O)C2=C(c3ccc(OCCOc4cc(F)ccc4Cl)cc3)C[C@@H]3CN(C(C)=O)C[C@H]2N3)C2CC2)cc(OC)c1.O=CO
Reaction #61355
(rac.)-(1R*,5S*)-3-Acetyl-7-{4-[2-(2-chloro-5-fluorophenoxy)ethoxy]phenyl}-3,9-diazabicyclo[3.3.1]non-6-ene-6-carboxylic acid cyclopropyl-(3,5-dimethoxybenzyl)amide formate salt
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ncc2ccc3c(C(N)=O)nn(C4CC5CCC(C4)N5C(=O)OCC(Cl)(Cl)Cl)c3c2n1
Reaction #74078
2,2,2-trichloroethyl 3-[3-carbamoyl-8-(methylsulfanyl)-1H-pyrazolo[4,3-h]quinazolin-1-yl]-8-azabicyclo[3.2.1]octane-8-carboxylate
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)Oc1cccc(C=O)c1
Reaction #76349
3-t-butoxybenzaldehyde
Выход 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)Oc1cc2c(cc1OC)CCN(CC(=O)NCc1ccccc1)C2Cc1ccc(OC)c(OC)c1
Reaction #77128
titled product
Выход 75.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)Oc1cccc(C=O)c1
Reaction #78783
3-t-butoxybenzaldehyde
Выход 32.0%DOI: 10.6084/m9.figshare.5104873.v1
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