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CCCC(O)CC(=O)O

CCCCCCCCCCC[C@H](CC(=O)OC)OCc1ccccc1
Reaction #5717
methyl (R)-3-(benzyloxy)-tetradecanoate
المردود 112.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@@H](O)CC(=O)O
Reaction #5718
(R)-3-hydroxytetradecanoic acid
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC(O)CC(=O)OCc1ccccc1
Reaction #53261
benzyl 6-methyl-3-hydroxyheptanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)C(=O)O[C@H]1C[C@H](O)C=C2C=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(=O)O)[C@H]21
Reaction #59804
Pravastatin
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@H](CC(=O)OC)OC(=O)C(Br)CCCCCC
Reaction #65817
(R)-3-[(2-bromo-1-oxooctyl)oxy]tetradecanoic acid methyl ester
المردود 87.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #65818
(R)-3-[2-bromo-1-oxooctyl)oxy
المردود 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@H](CC(=O)OC)OC(=O)CBr
Reaction #65822
(R)-3-[(bromoacetyl)oxy]tetradecanoic acid methyl ester
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75331
Hydrated hafnium-ammonium-gluconate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(O)CC(=O)OC
Reaction #84018
β-hydroxydodecanoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COCC2(COCc3ccc(OC)cc3)OC(=O)[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@@H]2OCc2ccccc2)cc1
Reaction #87466
(3R,4S,5S)-3,4,5-tris-benzyloxy-6,6-bis-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-2-one
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(c2ccc(Cl)c(Cc3ccc(O)cc3)c2)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #87468
product
المردود 33.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COCC2(COCc3ccc(OC)cc3)OC(=O)[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@@H]2OCc2ccccc2)cc1
Reaction #87486
(3R,4S,5S)-3,4,5-tris-benzyloxy-6,6-bis-(4-methoxy-benzyloxymethyl)-tetrahydro-pyran-2-one
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(c2ccc(Cl)c(Cc3ccc(O)cc3)c2)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Reaction #87488
product
المردود 33.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.[Na+]
Reaction #95431
sodium gluconate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CC[C@@H](C(=O)O)[C@@H](O)C1
Reaction #160379
(1R,2S,4R)-2-hydroxy-4-methyl-cyclohexanecarboxylic acid
المردود 94.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1C[C@H](C)CC[C@H]1C(=O)O
Reaction #160380
(1R,2S,4R)-2-Acetoxy-4-methyl-cyclohexanecarboxylic acid
المردود 53.4%DOI: 10.6084/m9.figshare.5104873.v1
NC1CCCC(C(=O)O)C1O
Reaction #162201
3-amino-2-hydroxy-cyclohexanecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(F)c(NC4CCCC(C(=O)O)C4O)n3)c3cc(Cl)cnc32)cc1
Reaction #162202
3-[[2-[5-chloro-1-(p-tolylsulfonyl)pyrrolo[2,3-b]pyridin-3-yl]-5-fluoro-pyrimidin-4-yl]amino]-2-hydroxy-cyclohexanecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=CO[C@H](CCc1ccccc1)[C@H](CCn1nnc2ccccc2c1=O)C(=O)O
Reaction #171199
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H](CCn1nnc2ccccc2c1=O)[C@H](O)CCc1ccccc1
Reaction #171200
title compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي