tert-butyllithium

O=C1CCCCCC12CCCC2
Reaction #1297
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCCCCC12CCCC2
Reaction #1433
desired product
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
CC(=O)c1ccc2c(c1)C(C)(C)CC=C2C(C)(C)C
Reaction #1484
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCc1cc2c(cc1C(=O)O)C(C)(C)CCC2(C)C
Reaction #1730
3-hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCOc1cc2c(cc1C(=O)Oc1ccc(C(=O)OCc3ccccc3)cn1)C(C)(C)CCC2(C)C
Reaction #1737
benzyl 6-(3-pentoxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-carbonyloxy)-nicotinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1c2c(c(C(O)(c3c4c(c(C(=O)OCC)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c4c(c(C(=O)OCC)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c1OC(C)(C)O3)OC(C)(C)O2
Reaction #2691
Bis-(8-ethoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiole-4-yl)-mono-(8-ethoxycarbonyl-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dioxol-4-yl)methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)Oc2c(c(C(O)(c3c4c(c(C(=O)O)c5c3OC(C)(C)O5)OC(C)(C)O4)c3c4c(c(C(=O)O)c5c3SC(C)(C)S5)SC(C)(C)S4)c3c(c2C(=O)O)OC(C)(C)O3)O1
Reaction #2694
Bis-(8-carboxy-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dioxol-4-yl)-mono-(8-carboxy-2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiol-4-yl) methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C2=CCC(C)(C)c3ccc(C=O)cc32)cc1
Reaction #2701
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C2=CCC(C)(C)c3ccc(C=O)cc32)s1
Reaction #2705
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C2=CC(C)(C)Sc3ccc(Br)cc32)cc1
Reaction #2710
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C2=CC(C)(C)Oc3ccc(C=O)cc32)cc1
Reaction #2712
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C2=CC(C)(C)Oc3ccc(C=O)cc32)s1
Reaction #2716
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1nc(C)c(C(=O)C(C)(C)C)o1
Reaction #2895
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOc1ccc2c(c1)c(-c1ccc3c(c1)OCO3)c(C(=O)OC)c(=O)n2Cc1ccccc1OC
Reaction #3003
methyl 4-(1,3-benzodioxol-5-yl)-1,2-dihydro-6-ethoxy-1-(2-methoxybenzyl)-2-oxoquinoline-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC[C@@H](C)C[C@@H](/C=C/[C@@H]1C(SCCCCCC(=O)OC)=C(OC(=O)C(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #3123
methyl(11R,12S,13E,15S,17R)-9-isobutyryloxy-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate
수율 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC[C@@H](/C=C/[C@@H]1C(SCCCCCC(=O)OC)=C(OC(=O)c2ccccc2)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #3127
methyl(11R,12S,13E,15S)-9-benzoyloxy-11,15-bis(tert-butyldimethylsiloxy)-7-thiaprosta-8,13-dienoate
수율 55.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)c1cc(C(F)(F)F)cc(Cl)c1C(=O)O
Reaction #3225
title compound
수율 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Clc1cc(C23CCCN2CCC3)cnc1Cl
Reaction #3386
oil
수율 54.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ncc(C23CCCN2CCC3)cn1
Reaction #3388
oil
수율 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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