Lawesson's reagent

CC(C)[C@H](NC(=O)OC(C)(C)C)C(N)=S
Reaction #3237
title compound
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1c(=S)c(-c2c(Cl)cccc2Cl)cc2cnc(N)nc21
Reaction #3269
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CC(CCCl)Sc2ncccc2C1=S
Reaction #4909
2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-thiazepine-5(4H)-thione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN1CC(CCCl)Oc2ccncc2C1=S.Cl
Reaction #4910
2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,4-f][1,4]oxazepine-5(4H)-thione monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN1CC(CCCl)Oc2ncc(Cl)cc2C1=S
Reaction #4912
7-Chloro-2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)thione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN1CC(CCC#N)Oc2ncccc2C1=S
Reaction #4914
product
Rendimiento 24.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cn1c(C#N)ccc1-c1ccc2c(c1)C1(CCCCC1)C(=S)N2
Reaction #9413
product
Rendimiento 90.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1(Cc2ccccc2)C(=S)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #9418
title compound
Rendimiento 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #9426
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)[C@@H]1CCC(=S)N1
Reaction #11048
title compound
Rendimiento 191.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(=S)n(-c2ccccc2)c1
Reaction #40702
1-phenyl-5-methyl-2-pyridinethione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cl.O=c1[nH]c(=S)ccn1CCCCN1C[C@@H]2C[C@]2(c2ccc(C(F)(F)F)cc2)C1
Reaction #41060
title compound
Rendimiento 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N[C@@H]1CC[C@@H](c2cccc(F)c2F)CNC1=S
Reaction #42666
title compound
Rendimiento 188.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2ccccc2)c(F)c2oc(C(N)=S)nc2c1C#N
Reaction #45767
compound
Rendimiento 41.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2ccccc2)c(CC(=S)N(C)C)c2oc(C3CC3)nc2c1C#N
Reaction #45884
compound
Rendimiento 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NC(=S)c1ccc(OC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc1
Reaction #46905
compound 6
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2cc(C(C)C(=O)Oc3ccc(C(N)=S)cc3)ccc2c1
Reaction #46910
compound 6
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)Cc1ccc(C(C)C(=O)Oc2ccc(C(N)=S)cc2)cc1
Reaction #46912
compound 4
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCC(N2CCCCC2=S)CC1
Reaction #48518
title compound
Rendimiento 128.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)OC(=O)N1c2cncnc2NC(=S)C1C
Reaction #49813
desired compound
Rendimiento 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
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