Abstract
Bis(BINOL) substituted 2,2′-bipyridines (1a and 1b ) have been prepared via a twofold Sonogashira
cross-coupling reaction from 3-iodo-2,2′-di(methoxymethoxy)-1,1′-binaphthyl
(4 ) and 5,5′-diethynyl-2,2′-bipyridine
(2 ), which could be synthesised through
a palladium mediated homodimerisation using zinc powder as a reducing
agent. 1a and 1b form
well defined silver(I ), copper(I) or zinc(II)
complexes [M1
2 ]+ and [Zn1a
2 ]2+ thereby
orienting the BINOL groups in a fashion potentially useful for molecular
recognition of chiral substrates.
Key words
cross-coupling reactions - palladium - ligands - complexes - supramolecular chemistry
References
<A NAME="RZ09902SS-1A">1a </A>
Noyori R.
Asymmetric
Catalysis in Organic Synthesis
John Wiley & Sons;
New
York:
1994.
<A NAME="RZ09902SS-1B">1b </A>
Noyori R.
Angew.
Chem., Int. Ed. Engl.
2002,
41:
2008 ; Angew. Chem. 2002 , 114, 2108
<A NAME="RZ09902SS-2A">2a </A>
Cram DJ.
Cram JM.
Acc.
Chem. Res.
1978,
11:
8
<A NAME="RZ09902SS-2B">2b </A>
Webb TH.
Wilcox CS.
Chem.
Soc. Rev.
1993,
22:
383
<A NAME="RZ09902SS-2C">2c </A>
Davis AP.
Wareham RS.
Angew.
Chem., Int. Ed. Engl.
1999,
38:
2978 ; Angew. Chem. 1999 , 111, 3160
<A NAME="RZ09902SS-2D">2d </A>
Hartley JH.
James TD.
Ward CJ.
J. Chem. Soc., Perkin Trans. 1
2000,
3155
<A NAME="RZ09902SS-3">3 </A>
Toda F. In Inclusion Compounds
Vol. 4:
Atwood JL.
Davies JED.
MacNicol DD.
Oxford University Press;
Oxford:
1991.
Chapter
4.
<A NAME="RZ09902SS-4">4 </A>
Pu L.
Chem.
Rev.
1998,
98:
2405
<A NAME="RZ09902SS-5">5 </A>
Lützen, A.; Thiemann, F.;
Meyer, S. Synthesis 2002 , submitted
for publication.
For reviews see:
<A NAME="RZ09902SS-6A">6a </A>
Lehn J.-M. Supramolecular Chemistry
VCH;
Weinheim:
1995.
p.139
<A NAME="RZ09902SS-6B">6b </A>
von Zelewsky A. Stereochemistry of
Coordination Compounds
John Wiley & Sons;
Chichester:
1995.
p.177
<A NAME="RZ09902SS-6C">6c </A>
Steed JW.
Atwood JL. Supramolecular Chemistry
John
Wiley & Sons;
Chichester:
2000.
p.463
<A NAME="RZ09902SS-6D">6d </A>
Albrecht M.
Chem.
Rev.
2001,
101:
3457
<A NAME="RZ09902SS-6E">6e </A>
Leininger S.
Olenyuk B.
Stang PJ.
Chem.
Rev.
2000,
100:
853
<A NAME="RZ09902SS-6F">6f </A>
Swiegers GF.
Malefetse TJ.
Chem.
Rev.
2000,
100:
3483
<A NAME="RZ09902SS-6G">6g </A>
Fujita M.
Umemoto K.
Yoshizawa M.
Fujita N.
Kusukawa T.
Biradha K.
Chem. Commun.
2001,
509
<A NAME="RZ09902SS-6H">6h </A>
Holliday BD.
Mirkin CA.
Angew.
Chem., Int. Ed. Engl.
2001,
40:
2022 ; Angew. Chem. 2001 , 113, 2076
<A NAME="RZ09902SS-7">7 </A>
Molecular modelling was performed using
commercially available PC Spartan Pro software
package from Wavefunction .
<A NAME="RZ09902SS-8">8 </A>
Grosshenny V.
Romero FM.
Ziessel R.
J.
Org. Chem.
1997,
62:
1491
<A NAME="RZ09902SS-9">9 </A>
Henze O.
Lehmann U.
Schlüter AD.
Synthesis
1999,
683
<A NAME="RZ09902SS-10">10 </A>
Schwab PFH.
Fleischer F.
Michl J.
J. Org. Chem.
2002,
67:
443
<A NAME="RZ09902SS-11">11 </A>
Lützen A.
Hapke M.
Eur. J. Org. Chem.
2002,
2292
<A NAME="RZ09902SS-12">12 </A>
Hama Y.
Nobuhara Y.
Aso Y.
Otsubo T.
Ogura F.
Bull. Chem.
Soc. Jpn.
1988,
61:
1683
<A NAME="RZ09902SS-13">13 </A>
Magidson G.
Menschikoff G.
Chem. Ber.
1925,
113
<A NAME="RZ09902SS-14">14 </A>
Baxter PNW.
J. Org. Chem.
2000,
65:
1257
<A NAME="RZ09902SS-15">15 </A>
Wolfe JP.
Singer RA.
Yang BH.
Buchwald SL.
J. Am. Chem. Soc.
1999,
121:
9550
<A NAME="RZ09902SS-16">16 </A>
The homodimerisation is usually finished
after a few hours as indicated by thin-layer chromatography. However prolonged
heating resulted in increased formation of by-products. Also change
of the solvent from DMF to THF gave only a mixture of unreacted
chloropyridine and 3 .
Recent reviews:
<A NAME="RZ09902SS-17A">17a </A>
Hassan J.
Sévignon M.
Gozzi C.
Schulz E.
Lemaire M.
Chem.
Rev.
2002,
102:
1359
<A NAME="RZ09902SS-17B">17b </A> Examples for Ni-catalyzed
homocoupling reactions of pyridines:
Amatore C.
Jutand A.
Acc. Chem. Res.
2000,
33:
314
<A NAME="RZ09902SS-17C">17c </A> See also:
Tiecco M.
Testaferri L.
Tingoli M.
Chianelli D.
Montanucci M.
Synthesis
1984,
736
<A NAME="RZ09902SS-17D">17d </A> See also:
Takagi K.
Hayama N.
Sasaki K.
Bull. Chem. Soc. Jpn.
1984,
57:
1887
<A NAME="RZ09902SS-17E">17e </A> See also:
Colon I.
Kelsey DR.
J. Org.
Chem.
1986,
51:
2627
<A NAME="RZ09902SS-17F">17f </A> See also:
Iyoda M.
Otsuka H.
Sato K.
Nisato N.
Oda M.
Bull.
Chem. Soc. Jpn.
1990,
63:
80
<A NAME="RZ09902SS-17G">17g </A> See also:
Fort Y.
Becker S.
Caubère P.
Tetrahedron
1994,
50:
11893
<A NAME="RZ09902SS-17H">17h </A>
See also: Janiak C.
Deblon S.
Wu H.-P.
Synth.
Commun.
1999,
29:
3341
Recent work on palladium catalysed
homocoupling reactions:
<A NAME="RZ09902SS-18A">18a </A>
Chan KS.
Tse AKS.
Synth.
Commun.
1993,
23:
1929
<A NAME="RZ09902SS-18B">18b </A>
Amatore C.
Carré E.
Jutand A.
Tanaka H.
Ren Q.
Torii S.
Chem.-Eur. J.
1996,
2:
957
<A NAME="RZ09902SS-18C">18c </A>
Jutand A.
Mosleh A.
J. Org. Chem.
1997,
62:
261
<A NAME="RZ09902SS-18D">18d </A>
Hassan J.
Penalva V.
Lavenot L.
Gozzi C.
Lemaire M.
Tetrahedron
1998,
54:
13793
<A NAME="RZ09902SS-18E">18e </A>
Venkatraman S.
Li C.-J.
Org. Lett.
1999,
1:
1133
<A NAME="RZ09902SS-18F">18f </A>
Hennings DD.
Iwarna T.
Rawal VH.
Org. Lett.
1999,
1:
1205
<A NAME="RZ09902SS-18G">18g </A>
Penalva V.
Hassan J.
Lavenot L.
Gozzi C.
Lemaire M.
Tetrahedron Lett.
1998,
39:
2559
<A NAME="RZ09902SS-18H">18h </A>
Hassan J.
Gozzi C.
Lemaire M.
C.
R. Acad. Sci. Ser IIc: Chim.
2000,
517
<A NAME="RZ09902SS-18I">18i </A>
Mukhopadhyay S.
Rothenberg G.
Gitis D.
Baidossi M.
Ponde DE.
Sasson Y.
J. Chem Soc., Perkin Trans.
2
2000,
2:
1809
<A NAME="RZ09902SS-19">19 </A> Enantiomerically pure BINOL was
obtained by resolution of racemic BINOL through clathrate formation
with N -benzylcinchonidinium chloride:
Hu Q.-S.
Vitharana D.
Pu L.
Tetrahedron: Asymmetry
1995,
6:
2123
<A NAME="RZ09902SS-20">20 </A> 2,2′-Di(methoxymethoxy)-1,1′-binaphthyl
has already been reported earlier, see:
Bähr A.
Droz AS.
Püntener M.
Neidlein U.
Anderson S.
Seiler P.
Diederich F.
Helv. Chim. Acta
1998,
81:
1931
We adapted a procedure published
by
<A NAME="RZ09902SS-21A">21a </A>
Matsunaga S.
Das J.
Roels J.
Vogl EM.
Yamamoto N.
Iida T.
Yamaguchi K.
Shibasaki M.
J. Am. Chem. Soc.
2000,
122:
2252
<A NAME="RZ09902SS-21B">21b </A> A TMEDA-free procedure
leading exclusively to 4 has also been
reported recently:
Liu TJ.
Chen YJ.
Zhang KS.
Wang D.
Guo DW.
Yang XZ.
Chirality
2001,
13:
595; however the yield of 4 ,
which can be obtained through this procedure is still in the same
order of magnitude
<A NAME="RZ09902SS-22">22 </A>
Hegedus LS. In Organometallics in Synthesis
Schlosser M.
John Wiley & Sons;
Chichester:
1997.
p.448
<A NAME="RZ09902SS-23">23 </A>
Unruh JD.
Christensen JR.
J. Mol. Catal.
1982,
14:
19
<A NAME="RZ09902SS-24">24 </A>
Suffert J.
J.
Org. Chem.
1989,
54:
509
<A NAME="RZ09902SS-25">25 </A>
Schwetlick K.
Organikum
21.
Ed.:
Wiley-VCH;
Weinheim:
2001.