ether

FC1(F)C=C(Cl)C1(F)Cl
Reaction #1662
colorless liquid
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1cccc(-c2ccccc2)nn1
Reaction #1665
desired product
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)NCCc1ccccc1
Reaction #1689
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)Cc1ccc([C@H]2CC[C@H](OC(=O)Cc3ccc(Cl)cc3)CC2)cc1.Cl
Reaction #1758
trans-O-(4-Chlorophenylacetyl)-4-(4-dimethylaminomethylphenyl)-cyclohexanol-hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)Cc1ccc([C@H]2CC[C@H](OC(=O)Cc3ccc(Cl)cc3)CC2)cc1.O=C([O-])C(O)C(O)C(=O)[O-]
Reaction #1759
trans-O-(4-Chlorophenylacetyl)-4-(4-dimethylaminomethylphenyl)-cyclohexanol tartrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=S(=O)(OCC(F)(F)F)C(F)(F)F
Reaction #1798
2,2,2-trifluoroethyltriflate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=S(=O)(OCC(F)(F)F)C(F)(F)F
Reaction #1799
2,2,2-trifluoroethyltriflate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(I)cc1
Reaction #1825
yellow solid
Ausbeute 99.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(CC(=O)O)NC(=O)OC(C)(C)C
Reaction #1831
product
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(CCCCCCCCOc2ccc(CO)nc2C=CC(=O)OC(C)(C)C)cc1
Reaction #1848
t-Butyl 3-{6-hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OC(c1ccccc1Cl)c1cc(Cl)ccc1NCC(F)(F)F
Reaction #1890
oily compound
Ausbeute 86.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#CC1(Cc2ccccc2)CCN(Cc2ccccc2)CC1
Reaction #1935
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(F)c(F)c(F)c(F)[n+]1[O-]
Reaction #1965
2-methyl-3,4,5,6-tetrafluoropyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
FC(F)(F)CNC1CCN(Cc2ccccc2)C1
Reaction #1980
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc(CN2CCC3CNCC3C2)cc1
Reaction #1989
title compound
Ausbeute 81.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)N1CCC[C@H]1[C@H](CCO)C[N+](=O)[O-]
Reaction #1992
3-(R)-(1-BOC-2-(S)-pyrrolidinyl)-4-nitrobutanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc(Cl)c1
Reaction #2162
3-(3-chlorobenzoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCC#CCOC1CCCCO1
Reaction #2164
4-tetrahydropyranoxy-2-butyn-1-ol
Ausbeute 68.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OCC#CC1CCCCC1
Reaction #2165
3-cyclohexyl-2-propyn-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
FC1(F)C=C(Cl)C1(F)Cl
Reaction #2167
colorless liquid
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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