References
<A NAME="RY00603ST-1A">1a</A>
Dolling U.-H.
Davis P.
Grabowski EJJ.
J. Am. Chem. Soc.
1984,
106:
446
<A NAME="RY00603ST-1B">1b</A> See also:
Bhattacharya A.
Dolling U.-H.
Grabowski EJJ.
Karady S.
Ryan KM.
Weinstock LM.
Angew. Chem., Int. Ed. Engl.
1986,
25:
476
<A NAME="RY00603ST-1C">1c</A>
Hughes DL.
Dolling U.-H.
Ryan KM.
Schoenewaldt EF.
Grabowski EJJ.
J. Org. Chem.
1987,
52:
4745
For reviews:
<A NAME="RY00603ST-2A">2a</A>
O’Donnell MJ. In
Catalytic Asymmetric Synthesis
Ojima I.
Verlag Chemie;
New York:
1993.
Chap. 8.
<A NAME="RY00603ST-2B">2b</A>
Shioiri T. In
Handbook of Phase-Transfer Catalysis
Sasson Y.
Neumann R.
Blackie Academic and Professional;
London:
1997.
Chap. 14.
<A NAME="RY00603ST-2C">2c</A>
Shioiri T.
Arai S. In Stimulating Concepts in Chemistry
Vogtle F.
Stoddart JF.
Shibasaki M.
Wiley-VCH;
Weinheim:
2000.
p.123
<A NAME="RY00603ST-2D">2d</A>
O’Donnell MJ.
Aldrichimica Acta
2001,
34:
3
<A NAME="RY00603ST-2E">2e</A>
Maruoka K.
Ooi T.
Chem. Rev.
2003,
103:
3013
For representative examples, see:
<A NAME="RY00603ST-3A">3a</A>
Lygo B.
Wainwright PG.
Tetrahedron Lett.
1997,
38:
8595
<A NAME="RY00603ST-3B">3b</A>
Corey EJ.
Xu F.
Noe MC.
J. Am. Chem. Soc.
1997,
119:
12414
<A NAME="RY00603ST-3C">3c</A>
Jew S.-S.
Jeong B.-S.
Yoo M.-S.
Huh H.
Park H.-G.
Chem. Commun.
2001,
1244
<A NAME="RY00603ST-3D">3d</A>
Chinchilla R.
Mazón P.
Nájera C.
Tetrahedron: Asymmetry
2002,
13:
927
<A NAME="RY00603ST-3E">3e</A>
Park H.-G.
Jeong B.-S.
Yoo M.-S.
Lee J.-H.
Park M.-K.
Lee Y.-J.
Kim M.-J.
Jew S.-S.
Angew. Chem. Int. Ed.
2002,
41:
3036
<A NAME="RY00603ST-3F">3f</A>
Jew S.-S.
Yoo M.-S.
Jeong B.-S.
Park Y.
Park H.-G.
Org. Lett.
2002,
4:
4245
1,1′-Binaphthyl derivatives:
<A NAME="RY00603ST-4A">4a</A>
Belokon YN.
Kochetkov KA.
Churkina TD.
Ikonnikov NS.
Chesnokov AA.
Larionov OV.
Parmar VS.
Kumar R.
Kagan HB.
Tetrahedron: Asymmetry
1998,
9:
851
<A NAME="RY00603ST-4B">4b</A>
Belokon YN.
Kochetkov KA.
Churkina TD.
Ikonnikov NS.
Vyskocil S.
Kagan HB.
Tetrahedron: Asymmetry
1999,
10:
1723
<A NAME="RY00603ST-4C">4c</A> Tartaric acid derivatives:
Shibuguchi T.
Fukuta Y.
Akachi Y.
Sekine A.
Ohshima T.
Shibasaki M.
Tetrahedron Lett.
2002,
43:
9539
<A NAME="RY00603ST-4D">4d</A>
Arai S.
Tsuji R.
Nishida A.
Tetrahedron Lett.
2002,
43:
9535
<A NAME="RY00603ST-4E">4e</A> Guanidine derivatives:
Kita T.
Georgieva A.
Hashimoto Y.
Nakata T.
Nagasawa K.
Angew. Chem. Int. Ed.
2002,
41:
2832
<A NAME="RY00603ST-4F">4f</A>
Nagasawa K.
Georgieva A.
Nakata T.
Tetrahedron
2001,
57:
8959
<A NAME="RY00603ST-4G">4g</A> Metal-salen complexes:
Belokon YN.
North M.
Kublitski VS.
Ikonnikov NS.
Krasik PE.
Maleev VI.
Tetrahedron Lett.
1999,
40:
6105
<A NAME="RY00603ST-4H">4h</A>
Belokon YN.
Davies RG.
North M.
Tetrahedron Lett.
2000,
41:
7245
For our recent contributions, see:
<A NAME="RY00603ST-5A">5a</A>
Ooi T.
Kameda M.
Maruoka K.
J. Am. Chem. Soc.
1999,
121:
6519
<A NAME="RY00603ST-5B">5b</A>
Ooi T.
Takeuchi M.
Kameda M.
Maruoka K.
J. Am. Chem. Soc.
2000,
122:
5228
<A NAME="RY00603ST-5C">5c</A>
Ooi T.
Kameda M.
Tannai H.
Maruoka K.
Tetrahedron Lett.
2000,
41:
8339
<A NAME="RY00603ST-5D">5d</A>
Ooi T.
Takeuchi M.
Maruoka K.
Synthesis
2001,
1716
<A NAME="RY00603ST-5E">5e</A>
Ooi T.
Uematsu Y.
Kameda M.
Maruoka K.
Angew. Chem. Int. Ed.
2002,
41:
1551
<A NAME="RY00603ST-5F">5f</A>
Ooi T.
Takahashi M.
Doda K.
Maruoka K.
J. Am. Chem. Soc.
2002,
124:
7640
<A NAME="RY00603ST-5G">5g</A>
Ooi T.
Taniguchi M.
Kameda M.
Maruoka K.
Angew. Chem. Int. Ed.
2002,
41:
4542
<A NAME="RY00603ST-5H">5h</A>
Ooi T.
Tayama E.
Maruoka K.
Angew. Chem. Int. Ed.
2003,
42:
579
<A NAME="RY00603ST-6">6</A>
Spectroscopic Characterization of 1b: [α]D
22 +156.2 (c 0.31, CHCl3). 1H NMR (400 MHz, CDCl3): δ = 7.37 (4 H, m, Ar-H), 7.21-7.32 (16 H, m, Ar-H), 7.14-7.19 (4 H, m, Ar-H), 7.04
(4 H, br d, J = 1.6 Hz, Ar-H), 3.87 (4 H, d, J = 13.2 Hz, ArCH2), 3.64 (4 H, d, J = 13.2 Hz, ArCH2), 2.18 (12 H, s, ArCH3), 1.68 (24 H, s, ArCCH3). 13C NMR (100 MHz, CDCl3): δ = 150.8, 149.7, 137.5, 135.5, 131.2, 128.2, 127.5, 126.7, 126.5, 125.8, 60.3,
42.9, 31.0, 30.5, 20.2. IR (KBr): 2963, 2928, 2870, 1740, 1680, 1601, 1495, 1445,
1383, 1364, 1232, 1202, 1097, 1076, 1030, 845, 768, 702 cm-1. HRMS (ESI-TOF): Calcd for C68H72N: 902.5659 (M+). Found: 902.5673 (M+).