diisobutylaluminum hydride

OCc1ccc(CCCC2OCCCO2)cc1
Reaction #985
alcohol
Выход 95.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1oc(-c2ccccc2)nc1COc1ccc2oc(/C=C/CO)cc2c1
Reaction #1157
(E)-3-[5-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]-2-propen-1-ol
Выход 90.0%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=CCc1ccc(Br)cc1
Reaction #1305
(4-bromophenyl)acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(C2(C#C[Si](C)(C)C)CCCC(=O)C2)cc1OC1CCCC1
Reaction #1403
3-(3-cyclopentyloxy-4-methoxyphenyl)-3-trimethylsilylethynyl cyclohexan-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=CCc1cccc(Br)c1
Reaction #1451
(3-bromophenyl)acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=CCc1ccc(Br)cc1
Reaction #1460
(4-bromophenyl)acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
OC1CCCc2ccc(OCc3ccncc3)cc21
Reaction #1706
Compound 2
Выход 78.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ncccc1CO
Reaction #1775
3-Hydroxymethyl-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=Cc1cc(OCOCCOC)c(OCOCCOC)c(Cl)c1Cl
Reaction #2675
expected product
Выход 99.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)C1(CCCN(C)CCc2ccccc2)C=CC=CC1CC=O
Reaction #4085
2-[3-[(Phenylethyl)methylamino]-propyl]-2-isopropylphenylacetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)=CCCC(C)=CC=C(C=O)C(C)C
Reaction #5760
2-(1-methylethyl)-5,9-dimethyl-2,4,8-decatrienal
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)=CCCC(C)=CCCC(C)=CC=C(C=O)C(C)C
Reaction #5762
2 -(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenal
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C/C1=C\C=C(\C(C)C)[C@@H](O)C/C(C)=C/CC/C(C)=C/CC1
Reaction #5767
sarcophytol A
Выход 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCCCCC[C@H](CC=O)OC1CCCCO1
Reaction #6151
(R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]tetradecanal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC1(C)CCC(C)(C)c2cc(OCc3ccc(C=O)cc3)ccc21
Reaction #6607
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
NCCC=Cc1ccccc1
Reaction #6810
4-phenyl-but-3-enylamine
Выход 79.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NCCc1c[nH]c2cc(O)ccc12
Reaction #6834
3-(2-amino-ethyl)-1H-indol-6-ol
Выход 68.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(CO)ccc1Br
Reaction #9727
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1c(-c2ccc(C(F)(F)F)cc2)csc1CO
Reaction #9737
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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