DCM

CC[C@H](NC(=O)[C@H](NC(=O)[C@@H](NC(=O)OCc1ccccc1)C(Cc1ccccc1)C(=O)O)[C@H](C)CC)c1ccccc1
Reaction #865
N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide
収率 33.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1c(S(N)(=O)=O)ccn1C
Reaction #911
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSc1c(S(N)(=O)=O)ccn1C
Reaction #913
title compound
収率 79.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1ccc(S(N)(=O)=O)c1Br
Reaction #915
title compound
収率 21.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CON=Cc1c(S(N)(=O)=O)ccn1C
Reaction #918
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)S(=O)(=O)c1c(S(N)(=O)=O)ccn1C
Reaction #920
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C(=O)c1c(S(N)(=O)=O)ccn1C
Reaction #922
title compound
収率 92.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C(CC)N=Cc1ccccc1
Reaction #945
desired product
収率 88.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
[N-]=[N+]=NCc1ccc(C(=N)NC(=O)OCc2ccccc2)cc1
Reaction #952
4-(benzyloxycarbonylamidino) benzyl azide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=CCCCc1ccccc1
Reaction #974
aldehyde
収率 22.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1cccc(Oc2ccccc2)c1
Reaction #976
aldehyde
収率 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C/C(C=O)=C\[C@H]1CC[C@H](O[Si](C)(C)C(C)(C)C)CC1
Reaction #977
aldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(C=O)cc1
Reaction #983
ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](OCc1ccc(CCCC2OCCO2)cc1)(c1ccccc1)c1ccccc1
Reaction #986
171
収率 102.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1CO[S@@](=O)N1c1ccccn1
Reaction #989
(R)-4-methyl-3-(2-pyridyl)-[1,2,3] oxathiazolidine 2-oxide
収率 599.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCl)Nc1ccccn1
Reaction #993
brown solid
収率 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc2[nH]cc(C(=O)C(Cl)(Cl)Cl)c12
Reaction #998
4-methoxy-3-trichloroacetyl-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(Cl)cncc1Cl
Reaction #1016
title compound
収率 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(COc1ccc(C#N)cc1)NC(=O)[C@@H](N)C(C)C.Cl
Reaction #1024
desired product
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(COc1ccc(C#N)cc1)NC(=O)[C@@H](NC(=O)Oc1ccccc1)C(C)C
Reaction #1025
white powder
収率 14.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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