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Extensive spectral tuning of the proton transfer emission from 550 to 675 nm via a rational derivatization of 10-hydroxybenzo[h]quinoline
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Formation of a one-dimensional stacking structure of -conjugated nitroxyl radical bearing a 1,2,5-thiadiazole ring and its magnetic property
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Interplay of weak interactions: An iridium(III) system with an agostic tert-butyl but a nonagostic isopropyl group
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Steric versus electronic effects of the ligand in the enantioselective palladium-catalyzed allylic alkylation with chiral oxazolinylpyridines
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19
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53149092028
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A general and efficient method for the synthesis of benzo-(iso)quinoline derivatives
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68949107860
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23
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0036774808
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NBuLi/lithium aminoalkoxide aggregates: New and promising lithiating agents for pyridine derivatives
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24
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0029059564
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Aggregative activation and heterocyclic chemistry III. Unusual regioselective lithiation of 2-alkoxy-pyridines
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33745400563
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Metallation versus heteroatom lithium complexation: Mono- and dilithiation of dipyridylpiperazines
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Excess of n-BuLi-LiDMAE was shown to be necessary with other substrates, see: (a) Louerat, F.; Gros, P.; Fort, Y. Metallation versus heteroatom lithium complexation: mono- and -dilithiation of dipyridylpiperazines. Synlett, 2006, 1379. (Pubitemid 43944613)
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28
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0037118360
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First direct lithiation of 2-pyridylpiperazine on solid phase
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29
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77951048339
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note
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3)2]), 180 (25), 151 (16).
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30
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34548780207
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The methyl group as a source of structural diversity in heterocyclic chemistry: Side chain functionalization of picolines and related heterocycles
-
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Mamane, V.; Aubert, E.; Fort, Y. The methyl group as a source of structural diversity in heterocyclic chemistry: side-chain functionalization of picolines and related heterocycles. J. Org. Chem., 2007, 72, 7294. (Pubitemid 47425498)
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Mamane, V.1
Aubert, E.2
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31
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77951079753
-
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note
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3) d 14.1, 22.6, 31.8, 38.7, 121.5, 124.2, 124.6, 125.2, 126.4, 126.6, 127.6, 127.8, 131.5, 133.6, 135.6, 145.8, 161.5; MS (EI) m/z 235 (7, M+), 193 (100).
-
-
-
-
32
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68949170982
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Direct 1,4-difunctionalization of isoquinoline
-
(a) Louerat, F.; Fort, Y.; Mamane, V. Direct 1,4-difunctionalization of isoquinoline. Tetrahedron Lett., 2009, 50, 5716.
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Louerat, F.1
Fort, Y.2
Mamane, V.3
-
33
-
-
0037020442
-
Enantioselective addition of organolithium reagents on isoquinoline
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DOI 10.1016/S0957-4166(02)00531-1, PII S0957416602005311
-
(b) Alexakis, A.; Amiot, F. Enantioselective addition of organolithium reagents on isoquinoline. Tetrahedron Asymmetry, 2002, 73, 2117. (Pubitemid 35217905)
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Alexakis, A.1
Amiot, F.2
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34
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77951035808
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Compound 11 is commercially available and can be purchased from Alfa Aesar
-
Compound 11 is commercially available and can be purchased from Alfa Aesar.
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-
-
-
35
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33845548031
-
A highly effective one-pot synthesis of quinolines from o-nitroarylcarbaldehydes
-
DOI 10.1039/b613775j
-
Li, A.-H.; Ahmed, E.; Chen, X.; Cox, M.; Crew, A. P.; Dong, H.-Q.; Jin, M.; Ma, L.; Panicker, B.; Siu, K. W.; Steinig, A. G.; Stolz, K. M.; Tavares, P. A. R.; Volk, B.; Weng, Q.; Werner, D.; Mulvihill, M. J. A highly effective one-pot synthesis of quinolines from o-nitroarylcarbaldehydes. Org. Biomol. Chem., 2007, 5, 61. (Pubitemid 44927101)
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Organic and Biomolecular Chemistry
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-
-
Li, A.-H.1
Ahmed, E.2
Chen, X.3
Cox, M.4
Crew, A.P.5
Dong, H.-Q.6
Jin, M.7
Ma, L.8
Panicker, B.9
Siu, K.W.10
Steinig, A.G.11
Stolz, K.M.12
Tavares, P.A.R.13
Volk, B.14
Weng, Q.15
Werner, D.16
Mulvihill, M.J.17
-
36
-
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77951037494
-
-
note
-
3) δ 9.32 (d, J = 8Hz, 1H), 8.19 (d, J = 8.6Hz, 1H), 8.03 (d, J = 8.6 Hz, 1H), 7.80-7.60 (m, 5H), 1.93 (s, 9H).
-
-
-
-
37
-
-
77951061657
-
-
note
-
11NOS: 253.0561, found 254.0634 (MH+).
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-
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