References
1
Modern
Amination Methods
Ricci A.
Wiley-VCH;
Weinheim:
2000.
2a
Yang BH.
Buchwald SL.
J. Organomet. Chem.
1999,
576:
125
2b
Wolfe JP.
Wagan S.
Marcoux J.-F.
Buchwald SL.
Acc.
Chem. Res.
1998,
31:
805
2c
Hartwig JF.
Angew. Chem. Int. Ed.
1998,
37:
2046
2d
Alcazar-Roman LM.
Hartwig JF.
Rheingold AL.
Liable-Sands LM.
Guzei IA.
J. Am. Chem. Soc.
2000,
122:
4618
3a
Klapars A.
Antilla JC.
Huang X.
Buchwald SL.
J. Am.
Chem. Soc.
2001,
123:
7727
3b
Wolter M.
Klapars A.
Buchwald SL.
Org.
Lett.
2001,
3:
3803
3c
Shen R.
Porco JA.
Org. Lett.
2000,
2:
1333
3d
Kalinin AV.
Bower JF.
Riebel P.
Snieckus V.
J. Org.
Chem.
1999,
64:
2986
For nickel-catalyzed aminations:
4a
Lipshutz BH.
Ueda H.
Angew. Chem.
Int. Ed.
2000,
39:
4492
4b
Desmarets C.
Schneider R.
Fort Y.
Tetrahedron
Lett.
2001,
42:
247
5
Sapountzis I.
Knochel P.
J. Am. Chem. Soc.
2002,
124:
9390
6a
Köbrich G.
Buck P.
Chem.
Ber.
1970,
103:
1412
6b
Yost Y.
Gutmann HR.
Muscoplat CC.
J. Chem. Soc. C
1971,
2119
7a
Jensen AE.
Dohle W.
Sapountzis I.
Lindsay DM.
Vu VA.
Knochel P.
Synthesis
2002,
265
7b
Rottländer M.
Boymond L.
Bérillon L.
Leprêtre A.
Varchi G.
Avolio S.
Laaziri H.
Quéguiner G.
Ricci A.
Cahiez G.
Knochel P.
Chem.-Eur. J.
2000,
6:
767
Recently, the utility of addition
reactions of silyl enol ethers to N=O-bonds has been demonstrated:
8a
Momoyama N.
Yamamoto H.
Angew. Chem. Int. Ed.
2002,
41:
2986
8b
Momoyama N.
Yamamoto H.
Org. Lett.
2002,
4:
3579
9 Analytical data of 3d:
Mp:
103-104 °C; 1H NMR (300 MHz,
CDCl3): δ [ppm] = 5.59
(br s, 1 H, NH), 6.73-6.76 (d, 3
J = 8.48 Hz, 2 H, CHarom.),
6.87-6.99 (m, 3 H, CHarom.), 7.18-7.23
(m, 2 H, CHarom.), 7.42-7.45 (d, 3
J = 8.48 Hz, 2 H, CHarom.); 13C
NMR (75 MHz, CDCl3): δ [ppm] = 82.07,
118.53, 119.25, 121.80, 129.42, 138.06, 142.16, 143.13; IR (KBr): [cm-1] = 3399
(s), 3054 (w), 3028 (w), 1932 (w), 1603 (s), 1581(vs), 1503(vs), 1482(vs),
1441 (m), 1387 (m), 1338 (w), 1315(vs), 1282 (m), 1238 (m), 1175
(m), 1154 (w), 1106 (w), 1078 (w), 1058 (w), 1027 (w), 1000 (w),
932 (w), 873 (w), 836 (m), 826 (m), 806 (m), 749 (s), 702 (m), 691
(s), 670 (w), 650 (w), 626 (w), 588 (w), 502 (m), 488 (w); MS (EI): m/z (I):
295 (100, M+), 167 (31), 139 (2), 84 (8), 77
(2); HRMS: calcd: 294.9858; found: 294.9856; C12H10IN:
calcd: C: 48.84; H: 3.42; N: 4.75; I: 43.00; found: C: 48.93; H:
3.40; N: 4.74; I: 42.99.