lithium hydroxide monohydrate

O=C(O)c1cccc(N2CCCCC2)c1
Reaction #2433
solid
收率 90.0%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 #2647
title compound
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O[C@@H]1C=C[C@H](OC2CCCCO2)C1
Reaction #2648
title compound
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2650
title compound
收率 101.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O[C@@H]1C=C[C@H](OCc2ccccc2)C1
Reaction #2652
title compound
收率 92.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@H](C[C@H](NC(=O)OC(C)(C)C)C(=O)O)C(=O)O
Reaction #2978
product
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)O)NC1=O
Reaction #5498
trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1N[C@H](C(=O)O)CSCCCCCCCC1CS
Reaction #5514
(3R)-6-mercaptomethyl-5-oxo-1-thia-4-azacyclotridecane-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1N[C@H](C(=O)N2C[C@H](O)C[C@H]2C(=O)O)CSCCCCCCCC1CS
Reaction #5518
trans N-[[(3R)-6-mercaptomethyl-5-oxo-1-thia-4-azacyclotridecan-3-yl]-carbonyl]-4-hydroxy-L-proline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1N[C@H](C(=O)O)CSCCCCCCCCC1CS
Reaction #5519
(3R)-6-mercaptomethyl-5-oxo-1-thia-4-azacyclotetradecane-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1cc(C(=O)NS(=O)(=O)c2ccccc2C#CCCCO)ccc1Cc1cn(C)c2ccc(NC(=O)OC3CCCC3)cc12
Reaction #6479
title compound
收率 97.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(O)[C@@H]1CCCC[C@@H]1NS(=O)(=O)c1ccc(Cl)cc1
Reaction #7125
product
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1nc2cc(OCc3cccc(F)c3)ccc2c(=O)n1CC(N)=O
Reaction #7725
title compound
收率 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(C(=O)O)ccc1-c1ccccn1
Reaction #7861
3-methoxy-4-pyridin-2-ylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(C(=O)O)ccc1CC#N
Reaction #7891
4-(cyanomethyl)-3-methoxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)c1ccc2c(-c3c(-c4ccccn4)nn4c3CCC4)ccnc2c1
Reaction #8331
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(O)C(=O)c1oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc2c1NC(=O)CO
Reaction #8897
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(O)C(=O)c1oc2nc(-c3ccccc3Cl)c(-c3ccc(Cl)cc3)cc2c1NC(=O)CO
Reaction #8912
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(C)ccc1C#N
Reaction #9015
2-methoxy-4-methylbenzonitrile
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1c(C)cccc1OC
Reaction #9038
ethyl 2-methoxy-6-methylbenzoate
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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