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OCc1csc2cncn12

OCc1c(Br)sc2c(-c3cccnc3)ncn12
Reaction #317216
2-bromo-7-(pyridin-3-yl)hydroxymethylimidazo[5,1-b]thiazole
DOI: 10.6084/m9.figshare.5104873.v1
CC[Si](CC)(CC)OCc1c(Br)sc2c(-c3cccnc3)ncn12
Reaction #317217
2-bromo-7-(pyridin-3-yl)triethylsilyloxymethylimidazo[5,1-b]thiazole
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1sc2c(-c3cccnc3)ncn2c1CO[Si](CC)(CC)CC
Reaction #317218
2-propionyl-7-(pyridin-3-yl)triethylsilyloxymethylimidazo[5,1-b]thiazole
Выход 79.8%DOI: 10.6084/m9.figshare.5104873.v1
CC[Si](CC)(CC)OCc1c(C(=O)C(C)[C@H]2NC(=O)[C@@H]2[C@@H](C)O[Si](C)(C)C(C)(C)C)sc2c(-c3cccnc3)ncn12
Reaction #317219
crude product
Выход 53.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(OC)c1ncn2c(-c3cccnc3)c(C(=O)[C@H](C)[C@H]3NC(=O)[C@@H]3[C@@H](C)O[Si](C)(C)C(C)(C)C)sc12
Reaction #317221
(3S,4R)-3-[(1R)-1-(tert-Butyldimethylsilyloxy)ethyl]-4-[(1R)-1-methyl-2-[7-dimethoxymethyl(pyridin-3-yl)imidazo[5,1-b]thiazol-2-yl]-2-oxoethyl]azetidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCc1csc2cncn12
Reaction #469778
3-(t-butyldi methylsilyloxy)methylimidazo[5,1-b]thiazole
Выход 98.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(O)c4csc5cncn45)C3)[C@H](C)[C@H]12
Reaction #655401
title compound
Выход 20.8%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)C1=C(S[C@H]2C[C@@H](C(O)c3csc4cn(C)c[n+]34)N(C(=O)OCC=C)C2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12.[I-]
Reaction #655402
allyl(1R,5S,6S)-6-((1R)-1-hydroxyethyl)-2-[(3S,5S)-1-allyloxycarbonyl-5-[1-hydroxy-1-(6-methylimidazo[5,1-b]thiazolium-3-yl)methyl]pyrrolidin-3-yl]thio-1-methylcarbapen-2-em-3-carboxylate iodide
Выход 95.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)C1=C(S[C@H]2C[C@@H](C(O)c3csc4cncn34)N(C(=O)OCC=C)C2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12
Reaction #655403
allyl(1R,5S,6S)-2-[(3S,5S)-1-allyloxycarbonyl-5-[1-hydroxy-1-(imidazo[5,1-b]thiazol-3-yl)methyl]pyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate
Выход 66.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(O)c4csc5cncn45)C3)[C@H](C)[C@H]12
Reaction #655404
colorless flocculent material
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)C1=C(S[C@H]2C[C@@H](C(O)c3csc4cn(C)c[n+]34)N(C(=O)OCC=C)C2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12.[I-]
Reaction #655405
allyl(1R,5S,6S)-2-[(3S,5S)-1-allyloxycarbonyl-5-[1-hydroxy-1-(6-methylimidazo[5,1-b]thiazolium-3-yl)methyl]pyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate iodide
Выход 97.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(O)c4csc5cn(C)c[n+]45)C3)[C@H](C)[C@H]12.[O-][Cl+3]([O-])([O-])[O-]
Reaction #655406
light orange flocculent material
Выход 68.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1C[C@H](O)C[C@H]1C(O)c1csc2cncn12
Reaction #655444
(3R,5S)-1-allyloxycarbonyl-3-hydroxy-5-[1-hydroxy-1-(imidazo[5,1-b]thiazol-3-yl)methyl]pyrrolidine
Выход 117.8%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1C[C@H](OS(C)(=O)=O)C[C@H]1C(O)c1csc2cncn12
Reaction #655445
(3R,5S)-1-allyloxycarbonyl-5-[1-hydroxy-1-(imidazo[5,1-b]thiazol-3-yl)methyl]-3-methanesulfonyloxypyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1C[C@@H](SC(C)=O)C[C@H]1C(O)c1csc2cncn12
Reaction #655446
title compound
Выход 72.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1C[C@H](O)C[C@H]1C(O)c1csc2cncn12
Reaction #655447
(3R,5S)-1-allyloxycarbonyl-3-hydroxy-5-[1-hydroxy-1-(imidazo[5,1-b]thiazol-3-yl)methyl]pyrrolidine
Выход 113.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1C[C@H](OS(C)(=O)=O)C[C@H]1C(O)c1csc2cncn12
Reaction #655448
(3R,5S)-1-allyloxycarbonyl-5-[1-hydroxy-(imidazo[5,1-b]thiazol-3-yl)methyl]-3-methanesulfonyloxypyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1C[C@@H](SC(C)=O)C[C@H]1C(O)c1csc2cncn12
Reaction #655449
title compound
Выход 41.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1C[C@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C(O)c1csc2cncn12
Reaction #655453
(3R,5S)-1-allyloxycarbonyl-3-t-butyldimethylsilyloxy-5-[1-hydroxy-1-(imidazo[5,1-b]thiazol-3-yl)methyl]pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)N1C[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1C(OC(C)=S)c1csc2cncn12
Reaction #655456
(3R,5R)-1-allyloxycarbonyl-3-t-butyldimethylsilyloxy-5-[1-(imidazo[5,1-b]thiazol-3-yl)-1-(methylthiocarbonyloxy)methyl]pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
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