類似構造検索

8722

CC(=O)SCC1CCCCCCC(CC(=O)OC(C)(C)C)C(=O)N1
Reaction #5500
10-(acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCC1CCCCCCC(CC(=O)OC(C)(C)C)C(=O)N1
Reaction #50255
10-(acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane
DOI: 10.6084/m9.figshare.5104873.v1
C[n+]1ccccc1F.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #517813
2-Fluoro-1-methylpyridinium 4-methylbenzenesulphonate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1050102
( 2 )
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C[n+]1ccccc1F.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #1076242
2-Fluoro-1-methylpyridinium 4-methylbenzenesulphonate
DOI: 10.6084/m9.figshare.5104873.v1
C[n+]1ccccc1F.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #1723089
2-Fluoro-1-methylpyridinium 4-methylbenzenesulphonate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)c1ccccc1
Reaction #1793463
benzyl benzoate
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
C[n+]1ccccc1F.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #1989928
2-fluoro-1-methylpyridinium tosylate
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(NC(=O)c2cc(-c3ccccn3)c(Cl)cc2Cl)n(-c2ccccc2)n1
Reaction #2087555
DOI: 10.1038/s41557
CCOC(=O)c1cc(NC(=O)c2cc(-c3ccccn3)c(Cl)cc2Cl)n(-c2ccccc2)n1
Reaction #2087571
DOI: 10.1038/s41557
CCOC(=O)c1cc(NC(=O)c2cc(-c3ccccn3)c(Cl)cc2Cl)n(-c2ccccc2)n1
Reaction #2087603
DOI: 10.1038/s41557
CCOC(=O)c1cc(NC(=O)c2cc(-c3ccccn3)c(Cl)cc2Cl)n(-c2ccccc2)n1
Reaction #2087619
DOI: 10.1038/s41557
CCOC(=O)c1cc(NC(=O)c2cc(-c3ccccn3)c(Cl)cc2Cl)n(-c2ccccc2)n1
Reaction #2087651
DOI: 10.1038/s41557
CCOC(=O)c1cc(NC(=O)c2cc(-c3ccccn3)c(Cl)cc2Cl)n(-c2ccccc2)n1
Reaction #2087667
DOI: 10.1038/s41557
CCOC(=O)c1cc(NC(=O)c2cc(-c3ccccn3)c(Cl)cc2Cl)n(-c2ccccc2)n1
Reaction #2087699
DOI: 10.1038/s41557
CCOC(=O)c1cc(NC(=O)c2cc(-c3ccccn3)c(Cl)cc2Cl)n(-c2ccccc2)n1
Reaction #2087715
DOI: 10.1038/s41557
CCOC(=O)CC[C@H](NC(=O)c1cc(C)c(CC[C@H]2CNc3nc(N)[nH]c(=O)c3C2)s1)C(=O)OCC
Reaction #2087737
DOI: 10.1038/s41557
CCOC(=O)CC[C@H](NC(=O)c1cc(C)c(CC[C@H]2CNc3nc(N)[nH]c(=O)c3C2)s1)C(=O)OCC
Reaction #2087740
DOI: 10.1038/s41557
CCOC(=O)CC[C@H](NC(=O)c1cc(C)c(CC[C@H]2CNc3nc(N)[nH]c(=O)c3C2)s1)C(=O)OCC
Reaction #2087763
DOI: 10.1038/s41557
CCOC(=O)CC[C@H](NC(=O)c1cc(C)c(CC[C@H]2CNc3nc(N)[nH]c(=O)c3C2)s1)C(=O)OCC
Reaction #2087786
DOI: 10.1038/s41557
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