Teilstruktursuche

C=CCI

—
Reaction #3760
diphenylmethyl ester
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCn1nc(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)c(Cc2ccc(CC)cc2)c1C
Reaction #7487
1-allyl-4-[(4-ethylphenyl)methyl]-3-(β-D-glucopyranosyloxy)-5-methyl-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(C(=O)OC(C)(C)C)CCc2ncc(NC(=O)OCc3ccccc3)c(=O)n21
Reaction #11070
intermediate 20a
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC[C@H](NC(=O)OC(C)(C)C)[C@H]1CO1
Reaction #48320
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)c1ccccc1)N(C(=O)c1ccccc1)C(C)(C)C
Reaction #49907
N-allyl-N'-t-butyl-N,N'-dibenzoylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
COC1(/C=C/CI)CCOCC1
Reaction #50181
4-methoxy-4-(3-iodo-trans-propenyl)tetrahydropyran
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)C(=NOC(F)F)c3csc(NC(c4ccccc4)(c4ccccc4)c4ccccc4)n3)[C@H]2S(=O)C1)[NH+]1CCCC1.[I-]
Reaction #62780
benzhydryl 7-[2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-(1-methyl-1-pyrrolidiniomethyl)-3-cephem-4-carboxylate-1-oxide iodide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(CI)CS(=O)[C@H]12)C(=NOC(F)F)c1csc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #62782
benzhydryl 7-[2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-iodomethyl-3-cephem-4-carboxylate-1-oxide
Ausbeute 42.4%DOI: 10.6084/m9.figshare.5104873.v1
Fc1c(F)c(COC2CCCCO2)c(F)c(F)c1CC=CCl
Reaction #62885
2-[4-(3-chloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyloxy]-tetrahydropyran
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C\CI
Reaction #62995
cis-7-Iodo-5-heptenoic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CN(C(=O)OC(C)(C)C)CCC1(OC)OC
Reaction #71934
title compound
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #81885
diphenylmethyl ester
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC1=CC=CC(OCCCC/C=C/c2ccc(OC)cc2)(C(C)=O)N1
Reaction #83542
6-acetyl-3-[6-(4-methoxyphenyl-(5E)-5-hexenyloxy]-2-pyridyl}-propionic acid methyl ester
Ausbeute 23.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(CP(=O)(OC)OC)CP(=O)(OC)OC
Reaction #95547
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1C(C)(c2cccc(Br)c2)COS1(=O)=O
Reaction #160456
3-allyl-4-(3-bromophenyl)-4-methyl-[1,2,3]-oxathiazolidine-2,2-dioxide
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(S(=O)(=O)OCCCC)CC1
Reaction #160575
titled product
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1ccc(O)cc1
Reaction #173074
DOI: 10.1039/C8SC04228D
C=CCn1c(=O)ccc2c1cc(F)c[n+]2[O-]
Reaction #174079
DOI: 10.1039/C8SC04228D
C=CCOc1cccc(C(=O)OC)c1
Reaction #176475
DOI: 10.1039/C8SC04228D
C=CCN1CCN(C(=O)OCc2ccccc2)CC1=O
Reaction #180150
DOI: 10.1039/C8SC04228D
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