zinc chloride

CCOC(=O)c1csc(-c2ccc3cc4c(cc3c2)C(C)(C)CCC4(C)C)c1
Reaction #1221
ethyl 2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthryl)-4-thiophenecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)OC(C)(C)C
Reaction #1271
Nε-dimethylamino-Nα-CBZ-O-t-butyl L-lysine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(/C=C/c2ccc3c(c2)C(c2nccs2)=CCC3(C)C)cc1
Reaction #1464
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
[Li][c]1cccs1
Reaction #1465
lithiothiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(N=Nc2ccc3c(c2)C(c2cccs2)=CCC3(C)C)cc1
Reaction #1481
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #1487
EtOAc hexanes
Ausbeute 5.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)O[C@H]1CC[C@H](c2ccc(CCl)cc2)CC1
Reaction #1746
trans-O-Acetyl-4-(4-chloromethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc(-c2nnn[nH]2)cc1
Reaction #1997
product
Ausbeute 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)O.C[C@]12CC[C@H](OCO)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #2080
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2639
title compound
Ausbeute 64.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCC[Si]1(c2ccccc2)CCC(c2cc(F)c(CC(C)CC)c(F)c2)CC1
Reaction #2743
4-(4-n-heptyl-4-phenyl-4-silacyclohexyl)-1-(2-methylbutyl)-2,6-difluorobenzene
Ausbeute 140.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Fc1cc(-c2ccsc2)cc(F)c1F
Reaction #3169
3(3,4,5-trifluorophenyl)thiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C1C(C)=CC(=O)CC1(C)C
Reaction #4075
ester
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCC#Cc1ccc(OC)cc1CCN(C)C.Cl
Reaction #4382
2-(1-hexynyl)-5-methoxy-N,N-dimethylbenzeneethanamine hydrochloride
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C1CCCc2[nH]c3ccc(Br)cc3c21
Reaction #4473
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)CC(C)(C)c1ccc(N)c([N+](=O)[O-])c1
Reaction #4807
4-tert-Octyl-2-nitroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2)SC[C@H]1OC(C)=O
Reaction #6088
expected product
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2)SC[C@H]1OC(C)=O
Reaction #6089
expected product
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1ccc(C#N)cc1
Reaction #6123
expected product
Ausbeute 112.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1ccc([N+](=O)[O-])cc1
Reaction #6130
expected product
Ausbeute 25.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
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