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1103413

Cn1c(=O)c(S(C)(=O)=O)c(O)c2ccccc21
Reaction #6787
white solids
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)c(S(C)(=O)=O)c(O)c2ccccc21
Reaction #42636
white solids
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(OC(=O)CS(=O)(=O)C(C)(C)C)CC(C)(C)N1
Reaction #54461
2,2,6,6-tetramethyl-4-piperidinyl t-butyl-sulphonyl-acetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(S(C)(=O)=O)CCC1
Reaction #58674
methyl 1-methylsulfonylcyclobutanecarboxlate
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)C1(C(=O)[O-])CCC1.[Li+]
Reaction #58675
lithium 1-methylsulfonylcyclobutanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCS(=O)(=O)CC(N)=O
Reaction #79572
acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCCC(CCCCCCC(=O)O)S(C)(=O)=O
Reaction #93915
title compound
Ausbeute 110.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCCC(CC#CCCCC(=O)O)S(C)(=O)=O
Reaction #93921
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)C(CCCCCCC(=O)O)CCCC(O)COc1ccc(F)cc1
Reaction #93931
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccc([N+](=O)[O-])cc1)C(=C(CBr)N1CCOCC1)N1C(=O)C2N=C(COc3ccccc3)SC21
Reaction #96111
p-nitrobenzyl α-[3-phenoxymethyl-7-oxo-4-thia-2,6-diazabicyclo[3,2,0]hept-2-en-6-yl]-α-(1-morpholino-2-bromoethylidene)acetate
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)O)S(=O)(=O)C1CCCCC1
Reaction #160412
2-cyclohexanesulfonyl-2-methyl-propionic acid
Ausbeute 95.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCSC(F)(F)F)S(=O)(=O)CCC(F)(F)C(F)(F)F
Reaction #167586
Ethyl 2-(3,3,4,4,4-Pentafluoro-butane-1-sulfonyl)-4-trifluoromethylsulfanyl-butyrate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCSC(F)(F)F)S(=O)(=O)CCC1(C)OCCO1
Reaction #167593
2-[2-(2-Methyl-[1,3]-dioxolan-2-yl)-ethanesulfonyl]-4-trifluoromethylsulfanyl-butyric acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(CCn1ccc(-c2ccccc2)cc1=O)S(C)(=O)=O
Reaction #171420
title compound
Ausbeute 61.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(Cl)c(F)c2F)cc1=O)(C(=O)O)S(C)(=O)=O
Reaction #171449
title compound
Ausbeute 89.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(CCn1ccc(-c2ccccc2)c(C)c1=O)S(C)(=O)=O
Reaction #171458
ethyl 2-methyl-4-(3-methyl-2-oxo-4-phenylpyridin-1(2H)-yl)-2-(methylsulfonyl)butanoate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)ccn(CCC(C)(C(=O)O)S(C)(=O)=O)c1=O
Reaction #171459
2-methyl-4-(3-methyl-2-oxo-4-phenylpyridin-1(2H)-yl)-2-(methylsulfonyl)butanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC)S(C)(=O)=O
Reaction #171463
solid
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC)(CCn1ccc(-c2ccccc2)cc1=O)S(C)(=O)=O
Reaction #171464
oil
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CCn1ccc(-c2ccccc2)cc1=O)(C(=O)O)S(C)(=O)=O
Reaction #171465
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
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