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620105

CN(C)Cc1ccc([C@H]2CC[C@H](OC(=O)Cc3ccc(Cl)cc3)CC2)cc1.O=C([O-])C(O)C(O)C(=O)[O-]
Reaction #1759
trans-O-(4-Chlorophenylacetyl)-4-(4-dimethylaminomethylphenyl)-cyclohexanol tartrate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H]1[C@@H](CC(=O)[O-])CC[C@H]1O
Reaction #2467
(1R,2S,3R)-3-hydroxy-2-pentyl-1-cyclopentaneacetate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccc(NC(C)=O)cc2)c1.O=C(O)C(O)C(O)C(=O)O
Reaction #2621
title compound
収率 75.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1(CCCN(C)CCc2ccccc2)C=CC=CC1CC=O
Reaction #4085
2-[3-[(Phenylethyl)methylamino]-propyl]-2-isopropylphenylacetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CC(CO)C1O)c1ccccc1
Reaction #6056
title compound
収率 101.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc(OCc3ccc(C=O)cc3)ccc21
Reaction #6607
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/C=C/C(=O)OCC
Reaction #6708
ethyl sorbate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](O)[C@@H](O)C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #7549
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol L-tartrate
収率 91.8%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/C=C/C(=O)OCC
Reaction #9835
ethyl sorbate
DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@H]2CCN(c3ccc(-c4ccc(-n5ncccc5=O)cc4)cc3)[C@H]2C1.O=C(O)[C@H](O)[C@@H](O)C(=O)O
Reaction #41236
title compound
収率 94.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1.O=C(O)C(O)C(O)C(=O)O
Reaction #43885
oseltamivir tartrate
収率 97.6%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/C=C/C(=O)OCC
Reaction #47125
ethyl sorbate
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@@H](O[Si](CC)(CC)CC)[C@@H](C)[C@H](O)[C@H](C)C=O
Reaction #50360
31
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(N)C(=O)N[C@H](COCc1ccccc1)C(=O)N1CCC2=NNC(=O)[C@]2(Cc2ccccc2)C1
Reaction #52063
2-amino-N-(2-(3a-(R)-benzyl-3-oxo-2,3,3a,4,6,7-hexahydro-pyrazolo[4,3-c]pyridin-5-yl)-1-(R)benzyloxymethyl-2-oxo-ethyl)isobutyramide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H](O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1OP(=O)(O)O
Reaction #52122
(R)-3-hydroxyoctanoyl-CoA
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)C(O)C(=O)O
Reaction #54862
racemic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc(C(=O)N[C@H]3CCCN(C(=O)OC(C)(C)C)C3)c(NC(N)=O)s2)cc1
Reaction #58613
light yellow solid
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc(C(=O)N[C@H]3CCCCN(C(=O)OC(C)(C)C)C3)c(NC(N)=O)s2)cc1
Reaction #58616
title compound
収率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccccc1-n1nc(OC2CCNCC2)c2ccccc21.O=C(O)[C@H](O)[C@@H](O)C(=O)O.O=C(O)[C@H](O)[C@@H](O)C(=O)O
Reaction #58693
L-tartrate salt—1-(2-fluoro-phenyl)-3-(piperidin-4-yloxy)-1H-indazole L-tartrate
収率 124.9%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)c1nnc2c(Br)cccc2c1N
Reaction #59368
title compound
収率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
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