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2673908

O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #1036
4-bromo-3-chloro-3,4,4-trifiuorobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(F)=C(F)F
Reaction #1038
3,4,4-trifluoro-3-butenoic
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(F)(Cl)C(F)(F)Cl
Reaction #1040
compound XI
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #1041
4-bromo-3-chloro-3,4,4-trifluorobutanoic acid
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H]1O[C@H](c2ccccc2Cl)c2cc(Cl)ccc2N(Cc2ccccc2)C1=O
Reaction #1880
trans-1-benzyl-7-chloro-5-(2-chlorophenyl)-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(=O)c(OCc2ccccc2)co1
Reaction #4203
product
Выход 5.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCCNC(=O)OC(CCC(=O)O)COC/C=C(\C)CCC=C(C)C
Reaction #5351
5-[((E)-3,7-dimethyl-2,6-octadienyl)oxy]-4-[[((Z)-9-octadecenylamino) carbonyl]oxy]pentanoic acid
Выход 30.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC[C@@H]1C[C@H](CC(=O)O)OC2(CCCCC2)O1
Reaction #5795
(±)-cis-4-(cyanomethyl)-1,5-dioxaspiro[5.5]undecane-2-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
N#CC[C@@H]1C[C@H](CC(=O)O)OCO1
Reaction #5800
(±)-cis-6-(cyanomethyl)-1,3-dioxane-4-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC1CC(=O)[C@@H](CCCCCC)C(=O)O1
Reaction #6154
tetrahydro-3-hexyl-4-oxo-(R)-6-undecyl-2H-pyran-2-one
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #6680
sulfuric acid ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(F)ccc1Oc1ccc(Cl)c(Cl)c1
Reaction #6996
2-(3,4-dichlorophenoxy)-5-fluoro-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NC(=O)c1ccccc1)[Si](C)(CCC(=O)O)c1ccccc1
Reaction #8643
3-[[1-(Benzoylamino)-3-methylbutyl]methylphenylsilyl]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CCCC(=O)O)CCN(C(=O)OC(C)(C)C)CC1
Reaction #8842
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)C1C(=O)CCC12CCN(C(=O)OC(C)(C)C)CC2
Reaction #8861
title compound
Выход 66.7%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(C2CCC2)c(Cl)nn1
Reaction #11321
title compound
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(Br)c(=O)[nH][nH]1
Reaction #43446
4-bromo-1,2-dihydro-3,6-pyridazinedione
Выход 151.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cc1cc(=O)[nH][nH]c1=O
Reaction #43453
solid
Выход 85.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #46040
sulfuric acid ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](OC(=O)OCc1ccccc1)[C@H]1C(=O)N[C@@H]1[C@@H](C)C(=O)O
Reaction #49998
(3S,4S)-4-(1-(R)-carboxyethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone
DOI: 10.6084/m9.figshare.5104873.v1
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