References and Notes
         <A NAME="RG02807ST-1A">1a</A> 
            
            Odom AL. 
            Dalton Trans. 
            2005, 
            225 
            
            
         <A NAME="RG02807ST-1B">1b</A> 
            
            Beller M. 
            
            Seayad J. 
            
            Tillack A. 
            
            Jiao H. 
            Angew. Chem. Int. Ed. 
            2004, 
            43: 
            3368 ; Angew. Chem. 2004, 116, 3448
            
         <A NAME="RG02807ST-1C">1c</A> 
            
            Alonso F. 
            
            Beletskaya IP. 
            
            Yus M. 
            Chem. Rev. 
            2004, 
            104: 
            3079 
            
            
         <A NAME="RG02807ST-1D">1d</A> 
            
            Doye S. 
            Synlett 
            2004, 
            1653 
            
            
         <A NAME="RG02807ST-1E">1e</A> 
            
            Pohlki F. 
            
            Doye S. 
            Chem. Soc. Rev. 
            2003, 
            32: 
            104 
            
            
         <A NAME="RG02807ST-1F">1f</A> 
            
            Bytschkov I. 
            
            Doye S. 
            Eur. J. Org. Chem. 
            2003, 
            935 
            
            
         <A NAME="RG02807ST-1G">1g</A> 
            
            Müller TE. 
            
            Beller M. 
            Chem. Rev. 
            1998, 
            98: 
            675 
            
            
         <A NAME="RG02807ST-2A">2a</A> 
            
            Anderson LL. 
            
            Arnold J. 
            
            Bergman RG. 
            Org. Lett. 
            2004, 
            6: 
            2519 
            
            
         <A NAME="RG02807ST-2B">2b</A> 
            
            Straub BF. 
            
            Bergman RG. 
            Angew. Chem. Int. Ed. 
            2001, 
            40: 
            4632 ; Angew. Chem. 
            2001, 113, 4768
            
         <A NAME="RG02807ST-2C">2c</A> 
            
            Johnson JS. 
            
            Bergman RG. 
            J. Am. Chem. Soc. 
            2001, 
            123: 
            2923 
            
            
         <A NAME="RG02807ST-2D">2d</A> 
            
            Baranger AM. 
            
            Walsh PJ. 
            
            Bergman RG. 
            J. Am. Chem. Soc. 
            1993, 
            115: 
            2753 
            
            
         <A NAME="RG02807ST-2E">2e</A> 
            
            Walsh PJ. 
            
            Baranger AM. 
            
            Bergman RG. 
            J. Am. Chem. Soc. 
            1992, 
            114: 
            1708 
            
            
         <A NAME="RG02807ST-2F">2f</A> For the first report of intermolecular hydroamination by titanium:  
            Hill JE. 
            
            Profilet RD. 
            
            Fanwick PE. 
            
            Rothwell IP. 
            Angew. Chem., Int. Ed. Engl. 
            1990, 
            29: 
            664 ; Angew. Chem. 1990, 102, 713
            
         <A NAME="RG02807ST-3A">3a</A> 
            
            Marcseková K. 
            
            Wegener B. 
            
            Doye S. 
            Eur. J. Org. Chem. 
            2005, 
            4843 
            
            
         <A NAME="RG02807ST-3B">3b</A> 
            
            Heutling A. 
            
            Pohlki F. 
            
            Bytschkov I. 
            
            Doye S. 
            Angew. Chem. Int. Ed. 
            2005, 
            44: 
            2951 ; Angew. Chem. 2005, 117, 3011
            
         <A NAME="RG02807ST-3C">3c</A> 
            
            Heutling A. 
            
            Severin R. 
            
            Doye S. 
            Synthesis 
            2005, 
            1200 
            
            
         <A NAME="RG02807ST-3D">3d</A> 
            
            Heutling A. 
            
            Pohlki F. 
            
            Doye S. 
            Chem. Eur. J. 
            2004, 
            10: 
            3059 
            
            
         <A NAME="RG02807ST-3E">3e</A> 
            
            Heutling A. 
            
            Doye S. 
            J. Org. Chem. 
            2002, 
            68: 
            1961 
            
            
         <A NAME="RG02807ST-4A">4a</A> 
            
            Cao C. 
            
            Li Y. 
            
            Shi Y. 
            
            Odom AL. 
            Chem. Commun. 
            2004, 
            2002 
            
            
         <A NAME="RG02807ST-4B">4b</A> 
            
            Shi Y. 
            
            Hall C. 
            
            Ciszewski JT. 
            
            Cao C. 
            
            Odom AL. 
            Chem. Commun. 
            2003, 
            586 
            
            
         <A NAME="RG02807ST-4C">4c</A> 
            
            Shi Y. 
            
            Ciszewski JT. 
            
            Odom AL. 
            Organometallics 
            2001, 
            20: 
            3967 
            
            
         <A NAME="RG02807ST-4D">4d</A> 
            
            Cao C. 
            
            Ciszewski JT. 
            
            Odom AL. 
            Organometallics 
            2001, 
            20: 
            5011 
            
            
         <A NAME="RG02807ST-5A">5a</A> 
            
            Lee AV. 
            
            Schafer LL. 
            Organometallics 
            2006, 
            25: 
            5249 
            
            
         <A NAME="RG02807ST-5B">5b</A> 
            
            Zhang Z. 
            
            Schafer LL. 
            Org. Lett. 
            2003, 
            5: 
            4733 
            
            
         <A NAME="RG02807ST-5C">5c</A> 
            
            Li C. 
            
            Thomson RK. 
            
            Gillon B. 
            
            Patrick BO. 
            
            Schafer LL. 
            Chem. Commun. 
            2003, 
            2462 
            
            
         <A NAME="RG02807ST-6A">6a</A> 
            
            Takaki K. 
            
            Koizumi S. 
            
            Yamamoto Y. 
            
            Komeyama K. 
            Tetrahedron Lett. 
            2006, 
            47: 
            7335 
            
            
         <A NAME="RG02807ST-6B">6b</A> 
            
            Buil ML. 
            
            Esteruelas MA. 
            
            López AM. 
            
            Mateo AC. 
            Organometallics 
            2006, 
            25: 
            4079 
            
            
         <A NAME="RG02807ST-6C">6c</A> 
            
            Esteruelas MA. 
            
            López AM. 
            
            Mateo AC. 
            
            Oñate E. 
            Organometallics 
            2006, 
            25: 
            1448 
            
            
         <A NAME="RG02807ST-6D">6d</A> 
            
            Hazari N. 
            
            Mountford P. 
            Acc. Chem. Res. 
            2005, 
            38: 
            839 
            
            
         <A NAME="RG02807ST-6E">6e</A> 
            
            Kaspar LT. 
            
            Fingerhut B. 
            
            Ackermann L. 
            Angew. Chem. Int. Ed. 
            2005, 
            44: 
            5972 ; Angew. Chem. 2005, 117, 6126
            
            
         <A NAME="RG02807ST-6F">6f</A> 
            
            Wang H. 
            
            Chan H.-S. 
            
            Xie Z. 
            Organometallics 
            2005, 
            24: 
            3772 
            
            
         <A NAME="RG02807ST-6G">6g</A> 
            
            Esteruelas MA. 
            
            López AM. 
            
            Mateo AC. 
            
            Oñate E. 
            Organometallics 
            2005, 
            24: 
            5084 
            
            
         <A NAME="RG02807ST-6H">6h</A> 
            
            Ackermann L. 
            
            Kaspar LT. 
            
            Gschrei CJ. 
            Org. Lett. 
            2004, 
            6: 
            2515 
            
            
         <A NAME="RG02807ST-6I">6i</A> 
            
            Ward BD. 
            
            Masse-François A. 
            
            Mountford P. 
            
            Gade LH. 
            Chem. Commun. 
            2004, 
            704 
            
            
         <A NAME="RG02807ST-6J">6j</A> 
            
            Lorber C. 
            
            Choukroun R. 
            
            Vendier L. 
            Organometallics 
            2004, 
            23: 
            1845 
            
            
         <A NAME="RG02807ST-6K">6k</A> 
            
            Ackermann L. 
            Organometallics 
            2003, 
            22: 
            4367 
            
            
         <A NAME="RG02807ST-6L">6l</A> 
            
            Ong T.-G. 
            
            Yap GPA. 
            
            Richeson DS. 
            Organometallics 
            2002, 
            21: 
            2839 
            
            
         <A NAME="RG02807ST-7A">7a</A> 
            
            Tillack A. 
            
            Khedkar V. 
            
            Jiao H. 
            
            Beller M. 
            Eur. J. Org. Chem. 
            2005, 
            5001 
            
            
         <A NAME="RG02807ST-7B">7b</A> 
            
            Khedkar V. 
            
            Tillack A. 
            
            Benisch C. 
            
            Melder J.-P. 
            
            Beller M. 
            J. Mol. Catal. A: Chem. 
            2005, 
            241: 
            175 
            
            
         <A NAME="RG02807ST-7C">7c</A> 
            
            Tillack A. 
            
            Khedkar V. 
            
            Beller M. 
            Tetrahedron Lett. 
            2004, 
            45: 
            8875 
            
            
         <A NAME="RG02807ST-7D">7d</A> 
            
            Kumar K. 
            
            Michalik D. 
            
            Garcia Castro I. 
            
            Tillack A. 
            
            Zapf A. 
            
            Arlt M. 
            
            Heinrich T. 
            
            Böttcher H. 
            
            Beller M. 
            Chem. Eur. J. 
            2004, 
            10: 
            746 
            
            
         <A NAME="RG02807ST-7E">7e</A> 
            
            Khedkar V. 
            
            Tillack A. 
            
            Beller M. 
            Org. Lett. 
            2003, 
            5: 
            4767 
            
            
         <A NAME="RG02807ST-7F">7f</A> 
            
            Beller M. 
            
            Breindl C. 
            
            Eichberger M. 
            
            Hartung CG. 
            
            Seayad J. 
            
            Thiel OR. 
            
            Tillack A. 
            
            Trauthwein H. 
            Synlett 
            2002, 
            1579 
            
            
         <A NAME="RG02807ST-7G">7g</A> 
            
            Seayad J. 
            
            Tillack A. 
            
            Hartung CG. 
            
            Beller M. 
            Adv. Synth. Catal. 
            2002, 
            344: 
            795 
            
            
         <A NAME="RG02807ST-7H">7h</A> 
            
            Tillack A. 
            
            Garcia Castro I. 
            
            Hartung CG. 
            
            Beller M. 
            Angew. Chem. Int. Ed. 
            2002, 
            41: 
            2541 ; Angew. Chem. 2002, 114, 2646
            
         <A NAME="RG02807ST-8A">8a</A> 
            
            Garcia Castro I. 
            
            Tillack A. 
            
            Hartung CG. 
            
            Beller M. 
            Tetrahedron Lett. 
            2003, 
            44: 
            3217 
            
            
         <A NAME="RG02807ST-8B">8b</A> 
            
            Haak E. 
            
            Bytschkov I. 
            
            Doye S. 
            Eur. J. Org. Chem. 
            2002, 
            457 
            
            
         <A NAME="RG02807ST-8C">8c</A> 
            
            Siebeneicher H. 
            
            Doye S. 
            Eur. J. Org. Chem. 
            2002, 
            1213 
            
            
         <A NAME="RG02807ST-9A">9a</A> 
            
            Ackermann L. 
            
            Born R. 
            Tetrahedron Lett. 
            2004, 
            45: 
            9541 
            
            
         <A NAME="RG02807ST-9B">9b</A> 
            
            Cao C. 
            
            Shi Y. 
            
            Odom AL. 
            Org. Lett. 
            2002, 
            4: 
            2853 
            
            
         For the general synthesis of indoles, see:
            
         <A NAME="RG02807ST-9C">9c</A> 
            
            Humphrey GR. 
            
            Kuethe JT. 
            Chem. Rev. 
            2006, 
            106: 
            2875 
            
            
         <A NAME="RG02807ST-9D">9d</A> 
            
            Gribble GW. 
            J. Chem. Soc., Perkin Trans. 1 
            2000, 
            1045 
            
            
         <A NAME="RG02807ST-10">10</A> 
            
            Moballigh A. 
            
            Jackstell R. 
            
            Beller M. 
            Tetrahedron Lett. 
            2004, 
            45: 
            869 
            
            
         <A NAME="RG02807ST-11">11</A> 
            
            Kumar K. 
            
            Zapf A. 
            
            Michalik D. 
            
            Tillack A. 
            
            Arlt M. 
            
            Beller M. 
            Org. Lett. 
            2004, 
            6: 
            7 
            
            
         <A NAME="RG02807ST-12A">12a</A> 
            
            Khedkar V. 
            
            Tillack A. 
            
            Michalik M. 
            
            Beller M. 
            Tetrahedron 
            2005, 
            61: 
            7622 
            
            
         <A NAME="RG02807ST-12B">12b</A> 
            
            Khedkar V. 
            
            Tillack A. 
            
            Michalik M. 
            
            Beller M. 
            Tetrahedron Lett. 
            2004, 
            45: 
            3123 
            
            
         <A NAME="RG02807ST-12C">12c</A> 
            
            Tillack A. 
            
            Jiao H. 
            
            Garcia Castro I. 
            
            Hartung CG. 
            
            Beller M. 
            Chem. Eur. J. 
            2004, 
            10: 
            2409 
            
            
         For selected recent syntheses of novel indole derivatives, see:
            
         <A NAME="RG02807ST-13A">13a</A> 
            
            Palimkar SS. 
            
            Kumar PH. 
            
            Lahoti RJ. 
            
            Srinivasan KV. 
            Tetrahedron 
            2006, 
            62: 
            5109 
            
            
         <A NAME="RG02807ST-13B">13b</A> 
            
            Terada Y. 
            
            Arisawa M. 
            
            Nishida A. 
            J. Org. Chem. 
            2005, 
            71: 
            1269 
            
            
         <A NAME="RG02807ST-13C">13c</A> 
            
            Hong KB. 
            
            Lee CW. 
            
            Yum EK. 
            Tetrahedron Lett. 
            2004, 
            45: 
            693 
            
            
         <A NAME="RG02807ST-13D">13d</A> 
            
            Köhling P. 
            
            Schmidt AM. 
            
            Eilbracht P. 
            Org. Lett. 
            2003, 
            5: 
            3213 
            
            
         <A NAME="RG02807ST-13E">13e</A> 
            
            Cacchi S. 
            
            Fabrizi G. 
            
            Parisi LM. 
            Org. Lett. 
            2003, 
            5: 
            3843 
            
            
         <A NAME="RG02807ST-13F">13f</A> 
            
            Siebeneicher H. 
            
            Bytschkov I. 
            
            Doye S. 
            Angew. Chem. Int. Ed. 
            2003, 
            42: 
            3042 ; Angew. Chem. 2003, 115, 3151
            
         <A NAME="RG02807ST-13G">13g</A> 
            
            Onitsuka K. 
            
            Suzuki S. 
            
            Takahashi S. 
            Tetrahedron  Lett. 
            2002, 
            43: 
            6197 
            
            
         <A NAME="RG02807ST-13H">13h</A> 
            
            Rutherford JF. 
            
            Rainka MP. 
            
            Buchwald SL. 
            J. Am. Chem Soc. 
            2002, 
            124: 
            15168 
            
            
         <A NAME="RG02807ST-13I">13i</A> 
            
            Tokunaga M. 
            
            Ota M. 
            
            Haga M. 
            
            Wakatsuki Y. 
            Tetrahedron Lett. 
            2001, 
            42: 
            3865 
            
            
         <A NAME="RG02807ST-13J">13j</A> 
            
            Verspui G. 
            
            Elbertse G. 
            
            Sheldon FA. 
            
            Hacking MAPJ. 
            
            Sheldon RA. 
            Chem. Commun. 
            2000, 
            1363 
            
            
         <A NAME="RG02807ST-13K">13k</A> 
            
            Beller M. 
            
            Breindl C. 
            
            Riermeier TH. 
            
            Eichberger M. 
            
            Trauthwein H. 
            Angew. Chem. Int. Ed. 
            1998, 
            37: 
            3389 ; Angew. Chem. 1998, 110, 3571
            <A NAME="RG02807ST-14">14</A>  
         For a recent review on Markovnikov and anti-Markovnikov functionalization of olefins
            and alkynes, see ref. 1b.
         For the synthesis of 3-phenoxy- and 3-methoxyindoles, see:
            
         <A NAME="RG02807ST-15A">15a</A> 
            
            Baccolini G. 
            
            Dalpozzo R. 
            
            Todesco PE. 
            J. Chem. Soc., Perkin Trans. 1 
            1988, 
            971 
            
            
         <A NAME="RG02807ST-15B">15b</A> 
            
            De Rosa M. 
            
            Carbognani L. 
            
            Febres A. 
            J. Org. Chem. 
            1981, 
            46: 
            2054 
            
            
         <A NAME="RG02807ST-15C">15c</A>  For the synthesis of 2-methylcarboxylate-3-(tert-butyl-dimethylsilyloxy)indole, see:  
            Malapel-Andrieu B. 
            
            Mérour J.-Y. 
            Tetrahedron 
            1998, 
            54: 
            11079 
            
            
         <A NAME="RG02807ST-16">16</A> 
            
            Kawashima Y. 
            
            Amanuma F. 
            
            Sato M. 
            
            Okuyama S. 
            
            Nakashima Y. 
            
            Sota K. 
            
            Moriguchi I. 
            J. Med. Chem. 
            1986, 
            29: 
            2284 
            
            
         <A NAME="RG02807ST-17">17</A> 
            
            Gormemis AE. 
            
            Ha TS. 
            
            Im I. 
            
            Jung K.-Y. 
            
            Lee JY. 
            
            Park V. 
            
            Kim Y.-C. 
            ChemBioChem 
            2005, 
            6: 
            1745 
            
            
         <A NAME="RG02807ST-18">18</A> For the silyl protection of propargyl alcohol, see:  
            Snider BB. 
            
            Shi Z. 
            J. Am. Chem. Soc. 
            1994, 
            116: 
            549 
            
            
         <A NAME="RG02807ST-19">19</A> 
            
            Schmidt AM. 
            
            Eilbracht P. 
            Org. Biomol. Chem. 
            2005, 
            3: 
            2333 
            
            
         <A NAME="RG02807ST-20">20</A> 
            
            Tietze LF. 
            
            Haunert F. 
            
            Feuerstein T. 
            
            Herzig T. 
            Eur. J. Org. Chem. 
            2003, 
            562 
            
            
         <A NAME="RG02807ST-21">21</A> 
            
            Bolm C. 
            
            Legros J. 
            
            Le Paih J. 
            
            Zani L. 
            Chem. Rev. 
            2004, 
            104: 
            6217 
            
            <A NAME="RG02807ST-22">22</A>  
         
            Representative Procedure: Synthesis of 1-Benzyl-3-(
            tert
            -butyldimethylsilyloxy)-2-methyl-1
            H
            -indole (4b)
            
In an ACE pressure tube under an argon atmosphere the ligand 2,6-di-tert-butyl-4-methylphenol (22.0 mg, 0.1 mmol) is dissolved in 3 mL dry toluene. To this
            solution N-benzyl-N-phenylhydrazine (257.7 mg, 1.3 mmol), tert-butyldimethylsiloxy-2-propyne (209.0 mL, 1.0 mmol) and Ti(NEt2)4 (18 µL, 0.05 mmol) were added. The reaction mixture was heated at 100 °C for 24 h.
            Then the pressure tube was opened under argon to add ZnCl2 (410.0 mg, 3.0 mmol). The reaction mixture was heated at 100 °C for further 24 h.
            After cooling to r.t. the solution was decanted and the dark residue was washed with
            toluene and EtOAc. After removal of the combined solvents in vacuo and purification by column chromatography (eluent: hexane-EtOAc = 10:1) yielded 1-benzyl-3-(tert-butyldimethyl-silyloxy)-2-methyl-1H-indole (175.8 mg, 50%) as light yellow solid (mp 69 °C). 1H NMR (300 MHz, CDCl3): δ = 7.45-7.40 (m, 1 H), 7.27-7.21 (m, 3 H, m-, p-Ph), 7.10 (m, 1 H), 6.93 (m, 2 H), 6.86-6.87 (m, 2 H, o-Ph), 5.22 (s, 2 H, CH2Ph), 2.20 (s, 3 H), 0.83 (s, 12 H), 0.15 (s, 6 H) ppm. 13C NMR (75 MHz, CDCl3): δ = 136.4 (i-Ph), 135.6, 133.6, 128.9 (m-Ph), 128.4, 127.8 (p-Ph), 125.8 (o-Ph), 121.7, 120.6, 120.8, 120.7, 108.7, 46.9, 25.8, 18.2, 9.1, -5.3 ppm. MS (EI,
            70 eV): m/z (relative intensity) = 351 (100) [M+], 294 (27), 260 (13), 221 (25), 204 (12), 177 (8), 115 (15), 91 (90), 73 (71), 65
            (8), 43 (6). HRMS (EI): m/z calcd for C22H29NOSi: 351.2013; found: 351.1999.