TBAF

CCOC(=O)c1csc(-c2ccc3cc(O)c(C45CC6CC(CC(C6)C4)C5)cc3c2)c1
Reaction #1241
ethyl 2-[7-(1-adamantyl)-6-hydroxy-2-naphthyl]-4-thiophenecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC1CCC(c2ccc(-c3ccc(F)c(F)c3)cc2)CC1
Reaction #1277
white crystals
収率 94.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CC1(O)CCC(C)(C)c2cc(C#Cc3ccc(C(=O)O)cc3)ccc21
Reaction #1336
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc2cc(-c3ccc4c(c3)C(O)CCC4(C)C)ccc2c1
Reaction #1456
Compound B4
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CC=C(c2cccs2)c2cc(C(=O)Oc3ccc(C(=O)O)cc3)ccc21
Reaction #1491
4-[[(5,5-Dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalen-2-yl)carbonyl]oxy]-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)CC(NCc1ccccc1CC(C(=O)O)N1C(=O)c2ccccc2C1=O)C(=O)OC(C)(C)C
Reaction #2811
title compound
収率 102.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1nc(C)c(C(O)(c2ccoc2)C(F)(F)F)o1
Reaction #2926
1-(2,4-Dimethyl-5-oxazolyl)-1-(3-furyl)-2,2,2-trifluoroethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=S(=O)(c1cc[c]([Bi]([c]2ccc(S(=O)(=O)N(CCO)CCO)cc2S(=O)(=O)N(CCO)CCO)[c]2ccc(S(=O)(=O)N(CCO)CCO)cc2S(=O)(=O)N(CCO)CCO)c(S(=O)(=O)N(CCO)CCO)c1)N(CCO)CCO
Reaction #2936
title compound
収率 94.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@@H]1C[C@@H](CO)N(C(=O)OC(C)(C)C)C1=O
Reaction #2976
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCC/C=C\CCCCCCCCNC(=O)OC(CCCO)COC/C=C(\C)CCC=C(C)C
Reaction #5350
(Z)-9-octadecenylcarbamic acid (E)-1-[[(3,7-dimethyl-2,6-octadienyl)oxy]methyl]-4-hydroxybutyl ester
収率 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C#CC[C@@]1(O)CC[C@@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(C(C)=O)cc3)C[C@@]21C
Reaction #5434
title compound
収率 69.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC1=CC=C(C(C)C)C(=O)CC(C)=CCCC(C)=CCC1
Reaction #5766
2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-cyclotetradecatetraen-1-one
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)OC(=O)CC(=O)C[C@H](O)CC#N
Reaction #5807
(R)-1,1-dimethylethyl 6-cyano-5-hydroxy-3-oxohexanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=C1C(CO)CC1OC(=O)c1ccccc1
Reaction #6054
title compound
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Nc1ccn([C@@H]2CS[C@H](CO)O2)c(=O)n1
Reaction #6520
3
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C#CC1=C(c2ccc(F)c(C)c2)CC(C)(C)CC1(C)C
Reaction #6617
1-(ethynyl)-2-(4-fluoro-3-methylphenyl)-4,4,6,6-tetramethyl-1-cyclohexene
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C#Cn1cnc2nc(NC(=O)C(C)(C)C)cc-2c1O
Reaction #6627
3-ethynyl-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1csc(S(N)(=O)=O)c1
Reaction #7058
title compound
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CSc1csc(S(N)(=O)=O)c1
Reaction #7061
title compound
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](NS(=O)(=O)/C=C/c2ccc(Cl)c(O)c2)C1=O
Reaction #7419
title compound
収率 83.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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