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[Hg]

OC1CCCCC2(C1)OCCO2
Reaction #1000
3-hydroxycycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc([N+](=O)[O-])cc2)SC[C@H]1OC(C)=O
Reaction #6092
expected product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc3ccccc3c2)SC[C@H]1OC(C)=O
Reaction #6094
expected product
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C(F)(F)F)cc2)SC[C@H]1OC(C)=O
Reaction #6095
expected product
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2cccc(C#N)c2)SC[C@H]1OC(C)=O
Reaction #6098
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccccc2C#N)SC[C@H]1OC(C)=O
Reaction #6101
expected product
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccccc2[N+](=O)[O-])SC[C@H]1OC(C)=O
Reaction #6103
expected product
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(S[C@@H]2SC[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]2OC(C)=O)cc(OC)c1OC
Reaction #6107
expected product
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2cccc([N+](=O)[O-])c2)SC[C@H]1OC(C)=O
Reaction #6108
expected product
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccccc2C(F)(F)F)SC[C@H]1OC(C)=O
Reaction #6110
expected product
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(-c3ccc(C#N)cc3)cc2)SC[C@H]1OC(C)=O
Reaction #6112
expected product
Ausbeute 10.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2cc(C(F)(F)F)cc(C(F)(F)F)c2)SC[C@H]1OC(C)=O
Reaction #6114
expected product
Ausbeute 35.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2C#N)SC[C@H]1OC(C)=O
Reaction #6116
expected product
Ausbeute 40.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2c(C#N)cc(C#N)cc2C#N)SC[C@H]1OC(C)=O
Reaction #6120
expected product
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #6174
liquid
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC[Si](C(=O)CC(C)C)(c1ccccc1)c1ccccc1
Reaction #8636
ketone
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC[Si](C)(C(=O)CC(C)C)c1ccccc1
Reaction #8640
ketone
DOI: 10.6084/m9.figshare.5104873.v1
C=COC1CCC=C1Br
Reaction #9365
1-bromo-5-vinyloxy-cyclopentene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(NS(=O)(=O)c1cccc(-c2cccc(Nc3nc4ccccc4[nH]3)c2)c1)c1ccccc1
Reaction #11043
Ethyl 3-{[3′-(1H-benzimidazol-2-ylamino)[1,1′-biphenyl]3-yl]-sulfonylamino}-3-phenyl-propanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)CN=C1NC[C@H](c2cccc(F)c2F)CC[C@H]1NC(=O)OC(C)(C)C
Reaction #42672
title compound
Ausbeute 108.5%DOI: 10.6084/m9.figshare.5104873.v1
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