部分構造検索

O=C([O-])O.[Na+]

COC(=O)c1c(N)ccc([N+](=O)[O-])c1C
Reaction #903
Methyl 2-methyl-3-nitro-6-aminobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C=O)cc1
Reaction #983
ester
DOI: 10.6084/m9.figshare.5104873.v1
BrC1CCCCCC12OCCO2
Reaction #999
2-bromocycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)cncc1Cl
Reaction #1016
title compound
収率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #1033
4-bromo-3-chloro-3,4,4-trifiuorobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nccc(NC2CCC(=Cc3ccc(Cl)cc3Cl)CC2)c1Cl
Reaction #1116
3-Chloro-4-[4-(2,4-dichlorobenzylidene)cyclohexyl]amino-2-ethylpyridine
収率 7.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nccc(N[C@H]2CC[C@@H](c3ccccc3)CC2)c1Br
Reaction #1119
2-Ethyl-3-bromo-4-(cis-4-phenylcyclohexylamino)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Clc1nccc(N[C@H]2CC[C@@H](c3ccccc3)CC2)c1Br
Reaction #1123
2-Chloro-3-bromo-4-(cis-4-phenylcyclohexylamino)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCn1ncc(C(=O)c2ccc3c(c2C)C(OC)CCS3(=O)=O)c1OC(=O)C1CCCCC1
Reaction #1162
4-methoxy-5-methyl-6-(5-cyclohexylcarbonyloxy-1-ethylpyrazol-4-yl)carbonylthiochroman-1,1-dioxide
収率 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC(O)COC1CCCCO1
Reaction #1219
1-(2-tetrahydropyranyloxy)-2-octadecanol
収率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=Cc2c(cccc2-c2cc3ccccc3c3ccccc23)C1
Reaction #1356
desired product
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC1Cc2c(Br)cccc2C1O[Si](C)(C)C
Reaction #1360
desired product
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CS[C@@H]1CN(C(=O)c2ccccc2)C[C@H]1N
Reaction #1411
1-Benzoyl-trans-3-amino-4-methylthio-pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN(C(=O)c2ccc([N+](=O)[O-])cc2)c2ccccc21
Reaction #1435
1-(4-nitrobenzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1472
crude material
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3O[Si](C)(C)C(C)(C)C)ccc2c1
Reaction #1473
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(C(=O)OCC)Oc2ccc(C[C@@H](C)N)cc2O1
Reaction #1622
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(CCN(Cc2ccccc2)C[C@H](O)COc2ccc(OCc3ccccc3)cc2)cc1
Reaction #1637
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=COCn1cnc2c(C(=O)N(c3ccccc3)c3ccccc3)nc(NC(C)=O)nc21
Reaction #1653
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)O)OCC1c2ccccc2-c2ccccc21
Reaction #1844
Fmoc-Gly-Pro-Hyp
DOI: 10.6084/m9.figshare.5104873.v1
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