tetrahydrofuran

COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #909
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #910
title compound
Yield 55.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSc1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #912
title compound
Yield 58.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1C=O
Reaction #916
title compound
Yield 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)S(=O)(=O)c1c(S(N)(=O)=O)c(C(C)(C)C)cn1C
Reaction #919
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #921
title compound
Yield 50.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1cccc1S(=O)(=O)NC(C)(C)C
Reaction #923
title compound
Yield 28.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccn(C)c1S(=O)(=O)NC(C)(C)C
Reaction #924
title compound
Yield 14.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(C)cc(Sc2cccc(F)c2C#N)c1
Reaction #941
2-Fluoro-6-[(3 -methyl-5-methoxyphenyl)thio]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(C)cc(Sc2cccc(N)c2C#N)c1
Reaction #942
2-Amino-6-[(3 -methyl-5-methoxyphenyl)thio]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(C)cc(S(=O)(=O)c2cccc(N)c2C#N)c1
Reaction #943
2-amino-6-[(3-methyl-5-methoxyphenyl)sulfonyl]benzonitrile
Yield 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC=CCC(N)(CC)CO
Reaction #946
desired product
Yield 32.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C(NC(=O)OCc1ccccc1)c1ccc(CN)cc1
Reaction #953
4-aminomethyl-1-(N-benzyloxycarbonylamidino)benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)CC1
Reaction #957
4-Aminoethyl-1-benzyloxycarbonylamidino piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NCCC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #968
title compound
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OC(CCCc1ccccc1)CCCc1ccccc1
Reaction #975
alcohol
Yield 88.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C/C(=C\[C@H]1CC[C@H](O[Si](C)(C)C(C)(C)C)CC1)C(O)CCCc1ccccc1
Reaction #978
alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCC(Cc1ccccc1)c1c[nH]c2ccccc12)CCC(Cc1ccccc1)c1c[nH]c2ccccc12
Reaction #980
ketone
Yield 68.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C(=C\c1ccccn1)/CC1OCCCO1
Reaction #981
E-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(C=CCC2OCCO2)cc1
Reaction #984
olefin
Yield 50.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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