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135260

CC1=C(C)[C@H]2[C@@H](C1)C[C@@]2(CN)CC(=O)O.Cc1ccc(S(=O)(=O)O)cc1
Reaction #638863
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C[C@@H]2[C@H](C1)C[C@]2(CN)CC(=O)O
Reaction #638866
solid
Ausbeute 77.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C[C@H]2[C@@H](C1)C[C@@]2(CN)CC(=O)O.O=S(=O)(O)c1ccccc1
Reaction #638867
solid
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C[C@H]2[C@@H](C1)C[C@@]2(CN)CC(=O)O
Reaction #638868
solid
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=CC2C(C1)CC2(CN)CC(=O)O.Cc1ccc(S(=O)(=O)O)cc1
Reaction #2278175
powder
Ausbeute 59.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C[C@@H]2[C@H](C1)C[C@]2(CN)CC(=O)OC(C)(C)C.Cc1ccc(S(=O)(=O)O)cc1
Reaction #2278177
tert-butyl [(1R*,5S*,6S*)-6-aminomethyl-3-ethylbicyclo[3.2.0]hept-3-en-6-yl]acetate p-toluenesulfonate
Ausbeute 80.6%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C[C@@H]2[C@H](C1)C[C@]2(CN)CC(=O)OC(C)(C)C
Reaction #2278178
tert-butyl [(1R*,5S*,6S*)-6-aminomethyl-3-ethylbicyclo[3.2.0]hept-3-en-6-yl]acetate
DOI: 10.6084/m9.figshare.5104873.v1