部分構造検索

454303

COCCOc1ccc(C(=O)O)cc1C
Reaction #160107
4-(2-methoxyethoxy)-3-methylbenzoic acid
収率 6.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OCCCS(=O)(=O)[O-])cc1.[Na+]
Reaction #345985
Sodium 3-(4-carbomethoxyphenoxy)propanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)CCCC.O=P([O-])(c1ccccc1)c1ccccc1
Reaction #346569
Tetra-n-butylphosphonium Diphenylphosphinate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)Oc1ccccc1)C(=O)O
Reaction #492127
N-phenoxycarbonyl-L-alanine
DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@H](NC(=O)Oc1ccccc1)C(=O)O
Reaction #492130
N-phenoxycarbonyl-L-methionine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OCCCS(=O)(=O)[O-])cc1.[Na+]
Reaction #522750
Sodium 3-(4-carbomethoxyphenoxy)propanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F.O=S(=O)([O-])C(F)(F)C(F)F
Reaction #578366
product
収率 109.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CCC(c2ccccc2)S(=O)(=O)N1Cc1ccc(N2CCC(n3cnnc3)CC2)cc1F
Reaction #604481
(3S)-2-[[2-fluoro-4-[4-(1,2,4-triazol-4-yl)-1-piperidyl]phenyl]methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide
収率 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)CCCC.O=P([O-])(c1ccccc1)c1ccccc1
Reaction #701760
Tetra-n-butylphosphonium Diphenylphosphinate
DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccc(C(=O)O)cc1C
Reaction #800192
4-(2-methoxyethoxy)-3-methylbenzoic acid
収率 6.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)CCCC.O=C(O)c1ccccc1O.O=C([O-])c1ccccc1O
Reaction #1009168
Tetrabutylphosphonium Salicylate Salicylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)C(=O)O.CC(O)C(=O)[O-].CCCC[P+](CCCC)(CCCC)CCCC
Reaction #1009172
Tetrabutylphosphonium Lactate lactic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C2CCC1(CS(=O)(=O)O)C(=O)C2.CCCC[P+](CCCC)(CCCC)CCCC.O=C([O-])c1ccccc1O
Reaction #1009173
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)C(=O)O.CCCC[P+](CCCC)(CCCC)CCCC.O=C([O-])c1ccccc1O
Reaction #1009174
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)CCCC.O=C(O)C=Cc1ccccc1.O=C([O-])c1ccccc1O
Reaction #1009175
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F.O=S(=O)([O-])C(F)(F)C(F)F
Reaction #1259155
product
収率 109.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F.O=S(=O)([O-])C(F)(F)C(F)F
Reaction #1259158
product
収率 109.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F.O=S(=O)([O-])C(F)(F)C(F)F
Reaction #1259161
product
収率 109.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F.O=S(=O)([O-])C(F)(F)C(F)F
Reaction #1259164
product
収率 109.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F.O=S(=O)([O-])C(F)(F)C(F)F
Reaction #1259167
product
収率 109.3%DOI: 10.6084/m9.figshare.5104873.v1
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