4-methylbenzenesulfonate

CC(C)[C@H](NCc1ccc(Br)cc1)C(=O)O
Reaction #40870
N-(4-bromobenzyl)-L-valine
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(S(=O)(=O)OCC2Cc3cc(C)c4c(c3O2)CCC4)cc1
Reaction #42204
(±)-(5-methyl-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methyl 4-methylbenzenesulfonate
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
[N-]=[N+]=NCC1Cc2ccc3ccccc3c2O1
Reaction #42207
(±)-2-(azidomethyl)-2,3-dihydronaphtho[1,2-b]furan
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(Cl)cc(CC(O)COS(=O)(=O)c2ccc(C)cc2)c1O
Reaction #42230
(±)-3-(5-chloro-2-hydroxy-3-methoxyphenyl)-2-hydroxypropyl 4-methylbenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
[N-]=[N+]=NCC1Cc2cc(Cl)c3ccccc3c2O1
Reaction #42248
(±)-(5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methyl azide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](C#CCCO)CC1
Reaction #53922
trans-[4-(4-Hydroxy-but-1-ynyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester
Ausbeute 107.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C=CCCCCC(COCCCCCCCCCCCCCCCC)OC
Reaction #64235
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Reaction #83935
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C1c2ccccc2C(=O)N1CCSCCc1ccco1
Reaction #94019
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
C=C1C2CCC(C2)C1(C)C=O
Reaction #158246
(1RS,2SR,4SR)-2-methyl-3-methylenebicyclo[2.2.1]heptane-2-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC=CC1OC(C(=O)OC(C)C)C(C(=O)OC(C)C)O1
Reaction #176661
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C2(C#Cc3ccccn3)CCC(=O)CC2)cc1OC1CCCC1
Reaction #177310
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)Oc1ccc(CC(NC(=O)OCc2ccccc2)C2OC(C)(C)OC2C(Cc2ccc(OC(C)(C)C)cc2)NC(=O)OCc2ccccc2)cc1
Reaction #179724
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)COC(c2ccc(C(C)(C)C)cc2C2OCCCO2)=N1
Reaction #180383
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CON=C(c1cc(C)on1)c1ccccc1CO
Reaction #180463
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(CC1CCCC1O)c1ccc(Cl)c(Cl)c1
Reaction #181618
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1ccc(Nc2ncnc3ccc(Oc4ccc(OCCCO)cn4)cc23)n1
Reaction #182006
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(C)OCc1cc(F)ccc1Br
Reaction #182293
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)COC(=O)C(C)OC(C)OC1CCCCC1
Reaction #182949
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C2OCC(C)(C)C(CO)O2)cc1
Reaction #184120
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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