tetrabutylammoniumbromide

CCCCC(CC)COCCCCCCCCCCOCC1CO1
Reaction #1193
10-(2-ethylhexyloxy)decyl glycidyl ether
Выход 82.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1C(=O)[C@@H](NC(=O)OCc2ccccc2)CSC[C@H]1c1ccccc1
Reaction #1284
(3R-cis)-Tetrahydro-5-oxo-3-phenyl-6-[[(phenylmethoxy)carbonyl]amino]-1,4-thiazepine-4(5H)-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CN1C(=O)[C@@H](NC(=O)OCc2ccccc2)CSC[C@H]1c1ccccc1
Reaction #1418
(3R-cis)-Tetrahydro-5-oxo-3-phenyl-6-[[(phenylmethoxy)carbonyl]amino]-1,4-thiazepine-4(5H)-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC[N+](CCCC)(CCCC)CCCC.O=C1N[C@H](c2ccccc2)CO1
Reaction #2420
(R)-4-phenyl-2-oxazolidinone tetra n-butylammonium salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=[N+]([O-])c1ccc(-n2nnnc2-c2ccccc2Br)cc1
Reaction #5773
5-(2-bromophenyl)-1-(4-nitrophenyl)-1H-tetrazole
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC(=O)N(CCCCCl)c1ccccc1N(CCCCCl)C(=O)CC
Reaction #6282
desired product
Выход 12.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
[N-]=[N+]=NCC1CCCP(=O)(Oc2ccccc2)O1
Reaction #6432
2-phenoxy-2-oxo-6-(azidomethyl)-1,2-oxaphosphorinane
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=COCCOc1ccc(C2CCCCC2)cc1
Reaction #6679
4-cyclohexylphenoxyethyl vinyl ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCC(c1cn(Cc2ccccc2)c2ccccc12)c1cn(Cc2ccccc2)c2ccccc12
Reaction #7044
product
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC1(COCCCCBr)COC1
Reaction #7425
3-[(4-bromobutoxy)methyl]-3-ethyloxetane
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc(C(OC2CN(CCCOCCc3ccc4sccc4c3)C2)(c2ccccc2)c2ccccc2)cc1
Reaction #7553
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-(trityloxy)azetidine
Выход 36.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(-c2nc3ccccc3o2)ccc1-c1cccnc1
Reaction #7857
2-(3-Methoxy-4-pyridin-3-ylphenyl)-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Clc1cc(-c2nc3ccccc3o2)ccc1-c1cccnc1
Reaction #7859
2-(3-Chloro-4-pyridin-3-ylphenyl)-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=S(=O)(c1ccccc1)n1cc(I)c2cc(F)cc(F)c21
Reaction #8210
N-Benzenesulfonyl-3-iodo-5,7-difluoroindole
Выход 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(Cc1cc(Cl)cc(Cl)c1)SC(C)(C)Cc1cc(Cl)cc(Cl)c1
Reaction #8497
( 4 )
Выход 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C(=CCOCc1ccccc1)COCc1ccccc1
Reaction #8505
( 18 )
Выход 114.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=NOCCN1CCOCC1)c1ccccc1
Reaction #10272
acetophenone O-[2-((morpholin-4-yl))ethyl]oxime
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1ccc(C(F)(F)F)cc1SC
Reaction #11003
6a
Выход 103.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1ccc(C(F)(F)F)cc1SC
Reaction #11004
6a
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1cc2cc(OC)cc(Br)c2o1
Reaction #11246
benzofuran
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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