hydrogen

Cc1c(N)ccc2c1C(=O)NS2(=O)=O
Reaction #905
4-Methyl-5-aminosaccharin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(N)cc1S(=O)(=O)NC(C)(C)C
Reaction #1093
N-tert-Butyl-5-amino-2-methoxycarbonylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1c(N(OCc2ccccc2)C2CCC3(CC2)OCC(C)(C)CO3)ccnc1C
Reaction #1098
4-[O-Benzyl-N-(3,3-dimethyl-1,5-dioxaspiro[5.5]undec-9-yl)hydroxylamino]-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCOc1cnc(-c2ccc(CCCCO)cc2)nc1
Reaction #1255
2-(4-(4-hydroxybutyl)-phenyl)-5-decyloxypyrimidine
المردود 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=CCc1cccc(Br)c1
Reaction #1301
(3-bromophenyl)acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1ccc2c(c1)CCC(O)C2
Reaction #1506
5,6,7,8-tetrahydro-6-hydroxynaphthalene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc2ccccc2c1
Reaction #1508
2-naphthalenecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCOc1ccc(C(=O)OC2CCc3cc(C(=O)O)ccc3C2)cc1
Reaction #1511
6-(4'-decyloxybenzoyloxy)-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCC[C@@H](OC(=O)C1CCc2cc(O)ccc2C1)C(F)(F)F
Reaction #1514
1,2,3,4-tetrahydro-6-hydroxynaphthalene-2-carboxylic acid (R)-1-trifluoromethylheptyl ester
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCOc1ccc2cc(C(=O)Oc3ccc(C(=O)O)cc3)ccc2c1
Reaction #1518
4-(6-decyloxy-2-naphthoyloxy)benzoic acid
المردود 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCOc1ccc(OC(=O)C2CCc3cc(O)ccc3C2)cc1
Reaction #1519
2-(4-decyloxyphenyloxycarbonyl)-1,2,3,4-tetrahydro-6-hydroxynaphthalene
المردود 97.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCC[C@@H](OC(=O)c1ccc(C(=O)O)cc1)C(F)(F)F
Reaction #1521
4-((R)-1-trifluoromethylheptyloxycarbonyl)benzoic acid
المردود 98.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCC[C@@H](C)OC(=O)c1ccc(C(=O)O)cc1
Reaction #1522
4-((R)-1-methylheptyloxycarbonyl)benzoic acid
المردود 99.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CN=CN(c2cc(N)c(F)cc2Cl)C1
Reaction #1562
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CNC(=O)Nc1ccc(F)c(N)c1
Reaction #1564
title product
المردود 60.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)OC(=O)Cn1c(=O)n(C)c(=O)n(-c2cc(N)c(F)cc2Cl)c1=O
Reaction #1568
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)Nc1cc(N)c(Cl)cc1F
Reaction #1575
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)C1Cc2cc(Cl)ccc2C1=O
Reaction #1599
desired product
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)C1Cc2cc(Cl)ccc2C1=O
Reaction #1666
desired product
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)C1NCCC2CCCCC21
Reaction #1685
perhydro-1-isoquinolinecarboxylic acid
المردود 56.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
الصفحة 1التالي