Teilstruktursuche

1217564

OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@H]1O
Reaction #7438
Gal
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #55561
methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1C[C@@H](NC=O)[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC13OCCOC12OCCO3
Reaction #70399
17,17-Bis(ethylendioxy)-7α-formamidoandrostane
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1-c1c2ccc(=O)cc-2oc2cc(O)ccc12
Reaction #335604
fluorescein
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1CCC(CCC2COCCO2)C1=O
Reaction #409681
2-4
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1CCC(CCC(C)=O)C1=O
Reaction #409682
2-5
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1[C@H](O)[C@H](NC)[C@H]2O[C@@]3(O)C(=O)C[C@@H](C)O[C@H]3O[C@@H]2[C@H]1O
Reaction #423211
Spectinomycin
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1-c1c2ccc(=O)cc-2oc2cc(O)ccc12
Reaction #741471
fluorescein
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #794928
α-olefins 1-pentadecene
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cc(F)c(=O)[nH]1
Reaction #1114508
5-FU
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CN1C(=O)[C@@H](N=[N+]=[N-])[C@H]1CCC(C)=O)OCCC(=O)OCc1ccccc1
Reaction #1119547
cis-1-(benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-(3-oxobutyl)-2-azetidinone
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #1527484
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
NCCC[C@H](N)C(=O)O
Reaction #1527485
L-ornithine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1CCC(CCC2COCCO2)C1=O
Reaction #1626898
DOI: 10.1039/C8SC04228D
CCOC(=O)CN1CCC(CCC2COCCO2)C1=O
Reaction #1689798
2-4
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1CCC(CCC(C)=O)C1=O
Reaction #1689799
2-5
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1-c1c2ccc(=O)cc-2oc2cc(O)ccc12
Reaction #1849905
fluorescein
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1C[C@@H](NC=O)[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC13OCCOC12OCCO3
Reaction #1999896
17,17-Bis(ethylendioxy)-7α-formamidoandrostane
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C[C@@H](NC=O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #1999897
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1[C@H](O)[C@H](NC)[C@H]2O[C@@]3(O)C(=O)C[C@@H](C)O[C@H]3O[C@@H]2[C@H]1O
Reaction #2078773
Spectinomycin
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter