بحث البنية الفرعية

701787

CCOC(=O)COC(C)COC
Reaction #47109
product 473
المردود 64.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COC(COc1ccccc1OCC)c1ccccn1
Reaction #174219
DOI: 10.1039/C8SC04228D
CCOC(=O)COC(C)C(=O)OCC
Reaction #180464
DOI: 10.1039/C8SC04228D
CCOC(=O)COC(C)COC
Reaction #188343
DOI: 10.1039/C8SC04228D
CCOC(=O)COC(COC(C)(C)C)C(OCc1ccccc1)[SiH](C)C
Reaction #286399
DOI: 10.1039/C8SC04228D
CCOC(=O)[C@H](C)O[C@@H](Cc1ccc(-c2cccc(Cl)c2)cc1)C(=O)O
Reaction #326099
(S)-3-(3′-chloro-biphenyl-4-yl)-2-((S)-1-ethoxycarbonyl-ethoxy)-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](C)O[C@@H](Cc1ccc(-c2cccc(Cl)c2)cc1)C(=O)O
Reaction #418858
(S)-3-(3′-chloro-biphenyl-4-yl)-2-((S)-1-ethoxycarbonyl-ethoxy)-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CO[C@@H](c2ccccc2)[C@@H](c2ccccc2)O1
Reaction #434511
2X
المردود 266.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CO[C@H](c1ccccc1)[C@@H](OC1CCCCO1)c1ccccc1
Reaction #434513
9S
المردود 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@@H](OC(C)=O)[C@H]1O[C@@](OC(C)=O)(C(=O)O)C[C@@H](OC(C)=O)[C@H]1OC(C)=O
Reaction #449355
20a
المردود 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](C)O[C@@H](Cc1ccc(-c2cccc(Cl)c2)cc1)C(=O)O
Reaction #476059
(S)-3-(3′-chloro-biphenyl-4-yl)-2-((S)-1-ethoxycarbonyl-ethoxy)-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COC(C(=O)OC)c1cn(C2CCCC2)c2cc(NC3CCCCC3)c(F)cc2c1=O
Reaction #556404
methyl [7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl](2-ethoxy-2-oxoethoxy)acetate
DOI: 10.6084/m9.figshare.5104873.v1
COC1C(OCC(=O)O)CCC2(CO2)C1C1(C)OC1CC=C(C)C
Reaction #568499
6-carboxymethoxy-5-methoxy-4-[2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-1-oxaspiro-[2,5]octane
المردود 91.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COC(C(=O)OC)C(=O)OC
Reaction #744274
desired product
المردود 100.1%DOI: 10.6084/m9.figshare.5104873.v1
COC1C(OCC(=O)O)CCC2(CO2)C1C1(C)OC1CC=C(C)C
Reaction #779310
DOI: 10.1039/C8SC04228D
C=CC(COC(c1ccccc1)(c1ccccc1)c1ccccc1)OCC(=O)OC(C)(C)C
Reaction #794883
tert-butyl 2-((1-(trityloxy)but-3-en-2-yl)oxy)acetate
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(COC(c1ccccc1)(c1ccccc1)c1ccccc1)OCC=O
Reaction #794884
2-((1-(trityloxy)but-3-en-2-yl)oxy)acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(C)CC(O)(C(=O)OCC)O1
Reaction #934563
product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]([C@H](CCc1ccccc1)c1ccc(Oc2ccccc2)cc1)N(CC(=O)O)C(=O)[C@]1(C(=O)O)OC[C@@H](C(=O)O)O1
Reaction #936538
(2S*,4S)-2-[N-(carboxymethyl)-N-{(1R,2R)-1-methyl-2-(4-phenoxyphenyl)-4-phenylbutyl}carbamoyl]-1,3-dioxolane-2,4-dicarboxylic acid
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(C(=O)OCC)O[C@@H](C(=O)OC(C)(C)C)[C@H](C(=O)N(CC(=O)OC(C)(C)C)[C@H](C)[C@H](CCc2ccccc2)c2ccc(Oc3ccccc3)cc2)O1
Reaction #936539
5-tert-butyl 2,2-diethyl (4R,5R)-4-[N-(tert-butoxycarbonylmethyl)-N-{(1R,2R)-1-methyl-2-(4-phenoxyphenyl)-4-phenylbutyl}carbamoyl]-1,3-dioxolane-2,2,5-tricarboxylate
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي