메뉴 건너뛰기




Volumn 19, Issue 10, 2014, Pages 16190-16222

Radical addition to iminium ions and cationic heterocycles

Author keywords

Addition reactions; Heterocycles; Iminium salts; Late stage functionalization; Minisci reaction; Photoredox catalysis; Porta reaction; Radicals; Rearrangements; Transition metal catalysis

Indexed keywords

CARBON; CATION; HETEROCYCLIC COMPOUND; ION;

EID: 84911921047     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules191016190     Document Type: Review
Times cited : (154)

References (115)
  • 2
    • 0001250845 scopus 로고
    • Nucleophilic character of alkyl radicals-VI: A new convenient selective alkylation of heteroaromatic bases
    • Minisci, F.; Bernardi, R.; Bertini, F.; Galli, R.; Perchinummo, M. Nucleophilic character of alkyl radicals-VI: A new convenient selective alkylation of heteroaromatic bases. Tetrahedron 1971, 27, 3575-3579.
    • (1971) Tetrahedron , vol.27 , pp. 3575-3579
    • Minisci, F.1    Bernardi, R.2    Bertini, F.3    Galli, R.4    Perchinummo, M.5
  • 3
    • 0034742750 scopus 로고    scopus 로고
    • Intermolecular addition of alkyl radicals to imines in the absence and in the presence of a Lewis acid
    • Halland, N.; Jorgensen, K.A. Intermolecular addition of alkyl radicals to imines in the absence and in the presence of a Lewis acid. J. Chem. Soc. 2001, 1290-1295.
    • (2001) J. Chem. Soc. , pp. 1290-1295
    • Halland, N.1    Jorgensen, K.A.2
  • 5
    • 0028908071 scopus 로고
    • Transition structures of hydride transfer-reactions of protonated pyridinium Ion with 1, 4-dihydropyridine and protonated nicotinamide with 1, 4-dihydronicotinamide
    • Wu, Y.D.; Lai, D.K.W.; Houk, K.N. Transition structures of hydride transfer-reactions of protonated pyridinium Ion with 1, 4-dihydropyridine and protonated nicotinamide with 1, 4-dihydronicotinamide. J. Am. Chem. Soc. 1995, 117, 4100-4108.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 4100-4108
    • Wu, Y.D.1    Lai, D.K.W.2    Houk, K.N.3
  • 7
    • 0040235878 scopus 로고
    • Homolytic aromatic arylation
    • Augood, D.R.; Williams, G.H. Homolytic aromatic arylation. Chem. Rev. 1957, 57, 123-190.
    • (1957) Chem. Rev. , vol.57 , pp. 123-190
    • Augood, D.R.1    Williams, G.H.2
  • 8
    • 33947343542 scopus 로고
    • The synthesis of biaryl compounds by means of the diazo reaction
    • Gomberg, M.; Bachmann, W.E. The synthesis of biaryl compounds by means of the diazo reaction. J. Am. Chem. Soc. 1924, 46, 2339-2343.
    • (1924) J. Am. Chem. Soc. , vol.46 , pp. 2339-2343
    • Gomberg, M.1    Bachmann, W.E.2
  • 9
    • 82455206185 scopus 로고    scopus 로고
    • Minisci reactions: Versatile CH-functionalizations for medicinal chemists
    • Duncton, M.A.J. Minisci reactions: Versatile CH-functionalizations for medicinal chemists. Med. Chem. Comm. 2011, 2, 1135-1161.
    • (2011) Med. Chem. Comm. , vol.2 , pp. 1135-1161
    • Duncton, M.A.J.1
  • 10
    • 4143121942 scopus 로고
    • Free-radical phenylations of 1-methyldiazoles
    • Lynch, B.M.; Chang, H.S. Free-radical phenylations of 1-methyldiazoles. Tetrahedron Lett. 1964, 5, 617-620.
    • (1964) Tetrahedron Lett. , vol.5 , pp. 617-620
    • Lynch, B.M.1    Chang, H.S.2
  • 11
    • 50549217384 scopus 로고
    • Concentration-dependent orientations in free-radical phenylations of heteroaromatic compounds
    • Lynch, B.M.; Chang, H.S. Concentration-dependent orientations in free-radical phenylations of heteroaromatic compounds. Tetrahedron Lett. 1964, 5, 2965-2968.
    • (1964) Tetrahedron Lett. , vol.5 , pp. 2965-2968
    • Lynch, B.M.1    Chang, H.S.2
  • 12
    • 50549196099 scopus 로고
    • Selective free-radical phenylations: Nitrogen-heteroaromatic compounds in acidic media
    • Dou, H.J.M.; Lynch, B.M. Selective free-radical phenylations: Nitrogen-heteroaromatic compounds in acidic media. Tetrahedron Lett. 1965, 6, 897-901.
    • (1965) Tetrahedron Lett. , vol.6 , pp. 897-901
    • Dou, H.J.M.1    Lynch, B.M.2
  • 13
    • 70349086814 scopus 로고
    • Méthylation radicalaire du thiazole et de ses derivés méthyles en milieu acétique
    • Dou, H.J.M. Méthylation radicalaire du thiazole et de ses derivés méthyles en milieu acétique. Bull. Soc. Chim. Fr. 1966, 5, 1678-1679.
    • (1966) Bull. Soc. Chim. Fr. , vol.5 , pp. 1678-1679
    • Dou, H.J.M.1
  • 14
    • 0008921503 scopus 로고
    • Phénylation radicalaire sélective en milieu acide-composés hétéroaromatiques azotes I. Methode et résultats expérimentaux
    • Dou, H.J.M.; Lynch, B.M. Phénylation radicalaire sélective en milieu acide-composés hétéroaromatiques azotes I. Methode et résultats expérimentaux. Bull. Soc. Chim. Fr. 1966, 12, 3815-3820.
    • (1966) Bull. Soc. Chim. Fr. , vol.12 , pp. 3815-3820
    • Dou, H.J.M.1    Lynch, B.M.2
  • 15
    • 70349137398 scopus 로고
    • Phénylation radicalaire sélective en milieu acide-composés hétéroaromatiques azotes 2. Traitement théorique des résultats expérimentaux et discussion
    • Dou, H.J.M.; Lynch, B.M. Phénylation radicalaire sélective en milieu acide-composés hétéroaromatiques azotes 2. Traitement théorique des résultats expérimentaux et discussion. Bull. Soc. Chim. Fr. 1966, 12, 3820-3823.
    • (1966) Bull. Soc. Chim. Fr. , vol.12 , pp. 3820-3823
    • Dou, H.J.M.1    Lynch, B.M.2
  • 16
    • 77956199653 scopus 로고    scopus 로고
    • Minisci reaction: A Friedel-Crafts type process with opposite reactivity and selectivity. Selective homolytic alkylation, acylation, carboxylation and carbamoylation of heterocyclic aromatic bases
    • Punta, C.; Minisci, F. Minisci reaction: A Friedel-Crafts type process with opposite reactivity and selectivity. Selective homolytic alkylation, acylation, carboxylation and carbamoylation of heterocyclic aromatic bases. Trends Heterocycl. Chem. 2008, 13, 1-68.
    • (2008) Trends Heterocycl. Chem. , vol.13 , pp. 1-68
    • Punta, C.1    Minisci, F.2
  • 18
    • 84897608614 scopus 로고    scopus 로고
    • Direct arylation of N-heteroarenes with aryldiazonium salts by photoredox catalysis in water
    • Xue, D.; Jia, Z.-H.; Zhao, C.-J.; Zhang, Y.-Y.; Wang, C.; Xiao, J. Direct arylation of N-heteroarenes with aryldiazonium salts by photoredox catalysis in water. Chem. Eur. J. 2014, 20, 2960-2965.
    • (2014) Chem. Eur. J. , vol.20 , pp. 2960-2965
    • Xue, D.1    Jia, Z.-H.2    Zhao, C.-J.3    Zhang, Y.-Y.4    Wang, C.5    Xiao, J.6
  • 19
    • 0001202624 scopus 로고
    • Recent developments of free-radical substitutions of heteroaromatic bases
    • Minisci, F.; Vismara, E.; Fontana, F. Recent developments of free-radical substitutions of heteroaromatic bases. Heterocycles 1989, 28, 489-519.
    • (1989) Heterocycles , vol.28 , pp. 489-519
    • Minisci, F.1    Vismara, E.2    Fontana, F.3
  • 20
    • 84986518972 scopus 로고
    • Substitutions by nucleophilic free-radicals-A new general reaction of heteroaromatic bases
    • Minisci, F.; Fontana, F.; Vismara, E. Substitutions by nucleophilic free-radicals-A new general reaction of heteroaromatic bases. J. Heterocycl. Chem. 1990, 27, 79-96.
    • (1990) J. Heterocycl. Chem. , vol.27 , pp. 79-96
    • Minisci, F.1    Fontana, F.2    Vismara, E.3
  • 21
    • 0037156631 scopus 로고    scopus 로고
    • Intramolecular radical additions to quinolines
    • Harrowven, D.C.; Sutton, B.J.; Coulton, S. Intramolecular radical additions to quinolines. Tetrahedron 2002, 58, 3387-3400.
    • (2002) Tetrahedron , vol.58 , pp. 3387-3400
    • Harrowven, D.C.1    Sutton, B.J.2    Coulton, S.3
  • 23
    • 77956695468 scopus 로고    scopus 로고
    • Radical additions to pyridines, quinolines and isoquinolines
    • Harrowven, D.C.; Sutton, B.J. Radical additions to pyridines, quinolines and isoquinolines. Prog. Heterocycl. Chem. 2004, 16, 27-53.
    • (2004) Prog. Heterocycl. Chem. , vol.16 , pp. 27-53
    • Harrowven, D.C.1    Sutton, B.J.2
  • 24
    • 34948892849 scopus 로고    scopus 로고
    • Synthesis using aromatic homolytic substitution-recent advances
    • Bowman, W.R.; Storey, J.M.D. Synthesis using aromatic homolytic substitution-recent advances. Chem. Soc. Rev. 2007, 36, 1803-1822.
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1803-1822
    • Bowman, W.R.1    Storey, J.M.D.2
  • 25
    • 84882263695 scopus 로고    scopus 로고
    • Radical-based regioselective C-H functionalization of electron-deficient heteroarenes: Scope, tunability, and predictability
    • O'Hara, F.; Blackmond, D.G.; Baran, P.S. Radical-based regioselective C-H functionalization of electron-deficient heteroarenes: Scope, tunability, and predictability. J. Am. Chem. Soc. 2013, 135, 12122-12134.
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 12122-12134
    • O'Hara, F.1    Blackmond, D.G.2    Baran, P.S.3
  • 26
    • 84971047361 scopus 로고
    • The synthesis of 2-alkyl- and 2-acyl-imidazoles by substitution methods
    • Begg, C.; Grimmett, M.; Yu-Man, L. The synthesis of 2-alkyl- and 2-acyl-imidazoles by substitution methods. Aust. J. Chem. 1973, 26, 415-420.
    • (1973) Aust. J. Chem. , vol.26 , pp. 415-420
    • Begg, C.1    Grimmett, M.2    Yu-Man, L.3
  • 27
    • 0031575588 scopus 로고    scopus 로고
    • Regiospecific alkylation of histidine and histamine at C-2
    • Jain, R.; Cohen, L.A.; El-Kadi, N.A.; King, M.M. Regiospecific alkylation of histidine and histamine at C-2. Tetrahedron 1997, 53, 2365-2370.
    • (1997) Tetrahedron , vol.53 , pp. 2365-2370
    • Jain, R.1    Cohen, L.A.2    El-Kadi, N.A.3    King, M.M.4
  • 28
    • 84862577822 scopus 로고    scopus 로고
    • Regiospecific direct C-H arylation at the 2-position of L-histidine using arylboronic acids
    • Mahindra, A.; Jain, R. Regiospecific direct C-H arylation at the 2-position of L-histidine using arylboronic acids. Synlett 2012, 1759-1764.
    • Synlett , vol.2012 , pp. 1759-1764
    • Mahindra, A.1    Jain, R.2
  • 31
    • 33748962264 scopus 로고
    • Radical carbamoylation of 1, 2, 3-triazinium 2-dicyanomethylides
    • Nagata, K.; Itoh, T.; Okada, M.; Takahashi, H.; Ohsawa, A. Radical carbamoylation of 1, 2, 3-triazinium 2-dicyanomethylides. Heterocycles 1991, 32, 855-857.
    • (1991) Heterocycles , vol.32 , pp. 855-857
    • Nagata, K.1    Itoh, T.2    Okada, M.3    Takahashi, H.4    Ohsawa, A.5
  • 34
    • 0025255381 scopus 로고
    • Intramolecular addition of Free radicals to quaternised heterocyclic rings
    • Murphy, J.A.; Sherburn, M.S. Intramolecular addition of Free radicals to quaternised heterocyclic rings. Tetrahedron Lett. 1990, 31, 1625-1628.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 1625-1628
    • Murphy, J.A.1    Sherburn, M.S.2
  • 35
    • 0025286263 scopus 로고
    • Intramolecular free-radical substitution reactions of pyridinium rings: Efficient formation of [5, 6]- and [6, 7]-fused ring systems
    • Murphy, J.A.; Sherburn, M.S. Intramolecular free-radical substitution reactions of pyridinium rings: Efficient formation of [5, 6]- and [6, 7]-fused ring systems. Tetrahedron Lett. 1990, 31, 3495-3496.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 3495-3496
    • Murphy, J.A.1    Sherburn, M.S.2
  • 36
    • 0036066526 scopus 로고    scopus 로고
    • N-Azinylpyridinium N-aminides: An approach to pyrazolopyridines via an intramolecular radical pathway
    • Nunez, A.; de Viedma, A.G.; Martinez-Barrasa, V.; Burgos, C.; Alvarez-Builla, J. N-Azinylpyridinium N-aminides: An approach to pyrazolopyridines via an intramolecular radical pathway. Synlett 2002, 1093-1096.
    • (2002) Synlett , pp. 1093-1096
    • Nunez, A.1    De Viedma, A.G.2    Martinez-Barrasa, V.3    Burgos, C.4    Alvarez-Builla, J.5
  • 37
    • 78651311363 scopus 로고    scopus 로고
    • Radical intramolecular arylation of pyridinium salts: A straightforward entry to 7-hydroxypyrido[2, 1-A]isoquinolinium salts
    • Castillo, R.R.; Burgos, C.; Vaquero, J.J.; Alvarez-Builla, J. Radical intramolecular arylation of pyridinium salts: A straightforward entry to 7-hydroxypyrido[2, 1-a]isoquinolinium salts. Eur. J. Org. Chem. 2011, 2011, 619-628.
    • (2011) Eur. J. Org. Chem. , vol.2011 , pp. 619-628
    • Castillo, R.R.1    Burgos, C.2    Vaquero, J.J.3    Alvarez-Builla, J.4
  • 38
    • 0343025849 scopus 로고
    • Umlagerung von N-Methyl-1.2-dihydropapaverin mit verdünnten Säuren
    • Knabe, J.; Kubitz, J.; Ruppenthal, A.N. Umlagerung von N-Methyl-1.2-dihydropapaverin mit verdünnten Säuren. Angew. Chem. 1963, 75, 981.
    • (1963) Angew. Chem. , vol.75 , pp. 981
    • Knabe, J.1    Kubitz, J.2    Ruppenthal, A.N.3
  • 39
    • 35648949767 scopus 로고
    • Über eine Umlagerung von N-Methyl-1 2-dihydropapaverin mit verdünnten Säuren
    • Knabe, J.; Kubitz, J. Über eine Umlagerung von N-Methyl-1, 2-dihydropapaverin mit verdünnten Säuren. Arch. Pharm. Ber. 1964, 297, 129-140.
    • (1964) Arch. Pharm. Ber. , vol.297 , pp. 129-140
    • Knabe, J.1    Kubitz, J.2
  • 40
    • 0019164766 scopus 로고
    • Dihydroisoquinoline rearrangement 27. Proposal of a new mechanism
    • Knabe, J.; Heckmann, R. Dihydroisoquinoline rearrangement 27. Proposal of a new mechanism, Arch. Pharm. 1980, 313, 1033-1042.
    • (1980) Arch. Pharm. , vol.313 , pp. 1033-1042
    • Knabe, J.1    Heckmann, R.2
  • 41
    • 49249150961 scopus 로고
    • Mechanism of the rearrangement of 1-benzyl-1, 2- dihydroisoquinolines-Some criticisms answered
    • Kinsman, R.G.; Dyke, S.F. Mechanism of the rearrangement of 1-benzyl-1, 2- dihydroisoquinolines-Some criticisms answered. Tetrahedron 1979, 35, 857-860.
    • (1979) Tetrahedron , vol.35 , pp. 857-860
    • Kinsman, R.G.1    Dyke, S.F.2
  • 43
    • 1842779942 scopus 로고
    • Evidence for a radical chain mechanism for the Knabe reaction of 1, 2-dihydro-2-methylpapaverine
    • Langhals, E.; Langhals, H.; Ruchardt, C. Evidence for a radical chain mechanism for the Knabe reaction of 1, 2-dihydro-2-methylpapaverine. Chem. Ber. 1984, 117, 1436-1454.
    • (1984) Chem. Ber. , vol.117 , pp. 1436-1454
    • Langhals, E.1    Langhals, H.2    Ruchardt, C.3
  • 44
    • 0023276642 scopus 로고
    • Rearrangement of dihydroisoquinolines 38. Behavior of 1, 2-dihydroisoquinolines with bulky C-1-substituents towards acids
    • Knabe, J.; Grunewald, F.J. Rearrangement of dihydroisoquinolines 38. Behavior of 1, 2-dihydroisoquinolines with bulky C-1-substituents towards acids. Arch. Pharm. 1987, 320, 492-499.
    • (1987) Arch. Pharm. , vol.320 , pp. 492-499
    • Knabe, J.1    Grunewald, F.J.2
  • 46
    • 0023217405 scopus 로고
    • Dihydroisoquinoline Rearrangement 39. 6, 7-Dimethoxy-2-methyl-1- (phenylpropargyl)-1, 2-dihydroisoquinoline
    • Knabe, J.; Hanke, B. Dihydroisoquinoline Rearrangement 39. 6, 7-Dimethoxy-2-methyl-1- (phenylpropargyl)-1, 2-dihydroisoquinoline. Arch. Pharm. 1987, 320, 629-635.
    • (1987) Arch. Pharm. , vol.320 , pp. 629-635
    • Knabe, J.1    Hanke, B.2
  • 47
    • 39849108423 scopus 로고
    • Dihydroisoquinoline rearrangement 9: Vinylog principle in rearrangement of tertiary 1, 2-dihydroisoquinolines
    • Knabe, J.; Holtje, H.D. Dihydroisoquinoline rearrangement 9: Vinylog principle in rearrangement of tertiary 1, 2-dihydroisoquinolines. Tetrahedron Lett. 1969, 10, 2107-2108.
    • (1969) Tetrahedron Lett. , vol.10 , pp. 2107-2108
    • Knabe, J.1    Holtje, H.D.2
  • 48
    • 0020544663 scopus 로고
    • Dihydroisoquinoline rearrangement 34. 7-Allyl-6-methyl-6, 7- dihydrothieno[2, 3-C]pyridine
    • Knabe, J.; Lorenz, J. Dihydroisoquinoline rearrangement 34. 7-Allyl-6-methyl-6, 7- dihydrothieno[2, 3-C]pyridine. Arch. Pharm. 1983, 316, 831-834.
    • (1983) Arch. Pharm. , vol.316 , pp. 831-834
    • Knabe, J.1    Lorenz, J.2
  • 49
    • 82255163444 scopus 로고    scopus 로고
    • 1, 3-Benzyl migration in iminium ions: Evidence for a fast free-radical chain reaction
    • Blank, N.; Straub, B.F.; Opatz, T. 1, 3-Benzyl migration in iminium ions: Evidence for a fast free-radical chain reaction. Eur. J. Org. Chem. 2011, 2011, 7355-7365.
    • (2011) Eur. J. Org. Chem. , vol.2011 , pp. 7355-7365
    • Blank, N.1    Straub, B.F.2    Opatz, T.3
  • 50
    • 0032705881 scopus 로고    scopus 로고
    • Direct oxidative carbon-carbon bond formation-using the "cation pool" method. 1. Generation of iminium cation pools and their reaction with carbon nucleophiles
    • Yoshida, J.; Suga, S.; Suzuki, S.; Kinomura, N.; Yamamoto, A.; Fujiwara, K. Direct oxidative carbon-carbon bond formation-using the "cation pool" method. 1. Generation of iminium cation pools and their reaction with carbon nucleophiles. J. Am. Chem. Soc. 1999, 121, 9546-9549.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 9546-9549
    • Yoshida, J.1    Suga, S.2    Suzuki, S.3    Kinomura, N.4    Yamamoto, A.5    Fujiwara, K.6
  • 52
    • 19744377011 scopus 로고    scopus 로고
    • Radical addition to "cation Pool". Reverse process of radical cation fragmentation
    • Maruyama, T.; Suga, S.; Yoshida, J.-I. Radical addition to "Cation Pool". Reverse process of radical cation fragmentation. J. Am. Chem. Soc. 2005, 127, 7324-7325.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 7324-7325
    • Maruyama, T.1    Suga, S.2    Yoshida, J.-I.3
  • 53
    • 33646924912 scopus 로고    scopus 로고
    • Distannane mediated reaction of N-acyliminium ion pools with alkyl halides. A chain mechanism involving radical addition followed by electron transfer
    • Maruyama, T.; Suga, S.; Yoshida, J.I. Distannane mediated reaction of N-acyliminium ion pools with alkyl halides. A chain mechanism involving radical addition followed by electron transfer. Tetrahedron 2006, 62, 6519-6525.
    • (2006) Tetrahedron , vol.62 , pp. 6519-6525
    • Maruyama, T.1    Suga, S.2    Yoshida, J.I.3
  • 54
    • 0001304781 scopus 로고
    • Kinetic applications of electron-paramagnetic resonance spectroscopy 27. Isomerization of cyclopropylcarbinyl to allylcarbinyl
    • Maillard, B.; Forrest, D.; Ingold, K.U. Kinetic applications of electron-paramagnetic resonance spectroscopy 27. Isomerization of cyclopropylcarbinyl to allylcarbinyl. J. Am. Chem. Soc. 1976, 98, 7024-7026.
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 7024-7026
    • Maillard, B.1    Forrest, D.2    Ingold, K.U.3
  • 55
    • 33847276108 scopus 로고    scopus 로고
    • Reactions of a N-acyliminium ion pool with benzylsilanes. Implication of a radical/cation/radical cation chain mechanism involving oxidative C-Si Bond Cleavage
    • Maruyama, T.; Mizuno, Y.; Shimizu, I.; Suga, S.; Yoshida, J.-I. Reactions of a N-acyliminium ion pool with benzylsilanes. Implication of a radical/cation/radical cation chain mechanism involving oxidative C-Si Bond Cleavage. J. Am. Chem. Soc. 2007, 129, 1902-1903.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 1902-1903
    • Maruyama, T.1    Mizuno, Y.2    Shimizu, I.3    Suga, S.4    Yoshida, J.-I.5
  • 56
    • 53649089093 scopus 로고    scopus 로고
    • Electro-initiated coupling reactions of N-acyliminium ion pools with arylthiomethylsilanes and aryloxymethylsilanes
    • Suga, S.; Shimizu, I.; Ashikari, Y.; Mizuno, Y.; Maruyama, T.; Yoshida, J. Electro-initiated coupling reactions of N-acyliminium ion pools with arylthiomethylsilanes and aryloxymethylsilanes. Chem. Lett. 2008, 37, 1008-1009.
    • (2008) Chem. Lett. , vol.37 , pp. 1008-1009
    • Suga, S.1    Shimizu, I.2    Ashikari, Y.3    Mizuno, Y.4    Maruyama, T.5    Yoshida, J.6
  • 57
    • 0035948184 scopus 로고    scopus 로고
    • Addition of carbon-centered radicals to imines and related compounds
    • Friestad, G.K. Addition of carbon-centered radicals to imines and related compounds. Tetrahedron 2001, 57, 5461-5496.
    • (2001) Tetrahedron , vol.57 , pp. 5461-5496
    • Friestad, G.K.1
  • 58
    • 2942702314 scopus 로고    scopus 로고
    • Carbon-carbon bond construction based on radical addition to C=N bond
    • Miyabe, H.; Ueda, M.; Naito, T. Carbon-carbon bond construction based on radical addition to C=N bond. Synlett 2004, 7, 1140-1157.
    • (2004) Synlett , vol.7 , pp. 1140-1157
    • Miyabe, H.1    Ueda, M.2    Naito, T.3
  • 59
    • 70049111044 scopus 로고    scopus 로고
    • Recent developments in nucleophilic radical addition to imines: The key role of transition metals and the new Porta radical-type version of the Mannich and Strecker reactions
    • Pastori, N.; Gambarotti, C.; Punta, C. Recent developments in nucleophilic radical addition to imines: The key role of transition metals and the new Porta radical-type version of the Mannich and Strecker reactions. Mini-Rev. Org. Chem. 2009, 6, 184-195.
    • (2009) Mini-Rev. Org. Chem. , vol.6 , pp. 184-195
    • Pastori, N.1    Gambarotti, C.2    Punta, C.3
  • 60
    • 77954948115 scopus 로고    scopus 로고
    • Progress in intermolecular carbon radical addition to imine derivatives
    • Miyabe, H.; Yoshioka, E.; Kohtani, S. Progress in intermolecular carbon radical addition to imine derivatives. Curr. Org. Chem. 2010, 14, 1254-1264.
    • (2010) Curr. Org. Chem. , vol.14 , pp. 1254-1264
    • Miyabe, H.1    Yoshioka, E.2    Kohtani, S.3
  • 61
    • 0032837567 scopus 로고    scopus 로고
    • Heteroatom radical addition-cyclization and its synthetic application
    • Naito, T. Heteroatom radical addition-cyclization and its synthetic application. Heterocycles 1999, 50, 505-541.
    • (1999) Heterocycles , vol.50 , pp. 505-541
    • Naito, T.1
  • 62
    • 0030666083 scopus 로고    scopus 로고
    • Free radical cyclizations involving nitrogen
    • Fallis, A.G.; Brinza, I.M. Free radical cyclizations involving nitrogen. Tetrahedron 1997, 53, 17543-17594.
    • (1997) Tetrahedron , vol.53 , pp. 17543-17594
    • Fallis, A.G.1    Brinza, I.M.2
  • 63
    • 0000977631 scopus 로고    scopus 로고
    • Indium-mediated intermolecular alkyl radical addition to electron-deficient C=N bond and C=C bond in water
    • Miyabe, H.; Ueda, M.; Nishimura, A.; Naito, T. Indium-mediated intermolecular alkyl radical addition to electron-deficient C=N bond and C=C bond in water. Org. Lett. 2002, 4, 131-134.
    • (2002) Org. Lett. , vol.4 , pp. 131-134
    • Miyabe, H.1    Ueda, M.2    Nishimura, A.3    Naito, T.4
  • 65
    • 0025332098 scopus 로고
    • Arylative amination of aldehydes promoted by aqueous titanium trichloride
    • Clerici, A.; Porta, O. Arylative amination of aldehydes promoted by aqueous titanium trichloride, Tetrahedron Lett. 1990, 31, 2069-2072.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 2069-2072
    • Clerici, A.1    Porta, O.2
  • 66
    • 84871548304 scopus 로고    scopus 로고
    • New advances in titanium-mediated free radical reactions
    • Rossi, B.; Prosperini, S.; Pastori, N.; Clerici, A.; Punta, C. New advances in titanium-mediated free radical reactions. Molecules 2012, 17, 14700-14732.
    • (2012) Molecules , vol.17 , pp. 14700-14732
    • Rossi, B.1    Prosperini, S.2    Pastori, N.3    Clerici, A.4    Punta, C.5
  • 67
    • 14844354033 scopus 로고    scopus 로고
    • One-pot four-component reaction: Aqueous TiCl3/PhN2+-mediated alkyl radical addition to imines generated in situ
    • Cannella, R.; Clerici, A.; Pastori, N.; Regolini, E.; Porta, O. One-pot four-component reaction: Aqueous TiCl3/PhN2+-mediated alkyl radical addition to imines generated in situ. Org. Lett. 2005, 7, 645-648.
    • (2005) Org. Lett. , vol.7 , pp. 645-648
    • Cannella, R.1    Clerici, A.2    Pastori, N.3    Regolini, E.4    Porta, O.5
  • 68
    • 27644539170 scopus 로고    scopus 로고
    • TiCl3/PhN2+-mediated radical addition of ethers to aldimines generated in situ under aqueous conditions
    • Clerici, A.; Cannella, R.; Panzeri, W.; Pastori, N.; Regolini, E.; Porta, O. TiCl3/PhN2+-mediated radical addition of ethers to aldimines generated in situ under aqueous conditions. Tetrahedron Lett. 2005, 46, 8351-8354.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 8351-8354
    • Clerici, A.1    Cannella, R.2    Panzeri, W.3    Pastori, N.4    Regolini, E.5    Porta, O.6
  • 69
    • 79955417186 scopus 로고    scopus 로고
    • New domino radical synthesis of aminoalcohols promoted by TiCl4-Zn/t-BuOOH system: Selective hydroxyalkylation of amines in alcohol or in cyclic ether cosolvents
    • Prosperini, S.; Pastori, N.; Ghilardi, A.; Clerici, A.; Punta, C. New domino radical synthesis of aminoalcohols promoted by TiCl4-Zn/t-BuOOH system: Selective hydroxyalkylation of amines in alcohol or in cyclic ether cosolvents. Org. Biomol. Chem. 2011, 9, 3759-3767.
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 3759-3767
    • Prosperini, S.1    Pastori, N.2    Ghilardi, A.3    Clerici, A.4    Punta, C.5
  • 70
    • 33747342194 scopus 로고    scopus 로고
    • A free radical Mannich type reaction: Selective α-CH aminomethylation of ethers by Ti(III)/t-BuOOH system under aqueous acidic conditions
    • Clerici, A.; Cannella, R.; Pastori, N.; Panzeri, W.; Porta, O. A free radical Mannich type reaction: Selective α-CH aminomethylation of ethers by Ti(III)/t-BuOOH system under aqueous acidic conditions. Tetrahedron 2006, 62, 5986-5994.
    • (2006) Tetrahedron , vol.62 , pp. 5986-5994
    • Clerici, A.1    Cannella, R.2    Pastori, N.3    Panzeri, W.4    Porta, O.5
  • 71
    • 84881617259 scopus 로고    scopus 로고
    • Light promoted aqueous phase amine synthesis via three-component coupling reactions
    • Zhang, L.; Deng, Y.Q.; Shi, F. Light promoted aqueous phase amine synthesis via three-component coupling reactions. Tetrahedron Lett. 2013, 54, 5217-5219.
    • (2013) Tetrahedron Lett. , vol.54 , pp. 5217-5219
    • Zhang, L.1    Deng, Y.Q.2    Shi, F.3
  • 72
    • 0141790814 scopus 로고    scopus 로고
    • Sunlight induced functionalisation of some heterocyclic bases in the presence of polycrystalline TiO2
    • Caronna, T.; Gambarotti, C.; Palmisano, L.; Punta, C.; Recupero, F. Sunlight induced functionalisation of some heterocyclic bases in the presence of polycrystalline TiO2. Chem. Commun. 2003, 18, 2350-2351.
    • (2003) Chem. Commun. , vol.18 , pp. 2350-2351
    • Caronna, T.1    Gambarotti, C.2    Palmisano, L.3    Punta, C.4    Recupero, F.5
  • 73
    • 77954933503 scopus 로고    scopus 로고
    • TiO2 in organic photosynthesis: Sunlight induced functionalization of heterocyclic bases
    • Gambarotti, C.; Punta, C.; Recupero, F.; Caronna, T.; Palmisano, L. TiO2 in organic photosynthesis: Sunlight induced functionalization of heterocyclic bases. Curr. Org. Chem. 2010, 14, 1153-1169.
    • (2010) Curr. Org. Chem. , vol.14 , pp. 1153-1169
    • Gambarotti, C.1    Punta, C.2    Recupero, F.3    Caronna, T.4    Palmisano, L.5
  • 74
    • 58149156300 scopus 로고    scopus 로고
    • A new one-pot, four-component synthesis of 1, 2-amino alcohols: TiCl3/t-BuOOH-mediated radical hydroxymethylation of imines
    • Clerici, A.; Ghilardi, A.; Pastori, N.; Punta, C.; Porta, O. A new one-pot, four-component synthesis of 1, 2-amino alcohols: TiCl3/t-BuOOH-mediated radical hydroxymethylation of imines. Org. Lett. 2008, 10, 5063-5066.
    • (2008) Org. Lett. , vol.10 , pp. 5063-5066
    • Clerici, A.1    Ghilardi, A.2    Pastori, N.3    Punta, C.4    Porta, O.5
  • 75
    • 76449100485 scopus 로고    scopus 로고
    • Efficient radical domino approach to β-aminoalcohols from arylamines and alcohols triggered by Ti(III)/t-BuOOH
    • Spaccini, R.; Ghilardi, A.; Pastori, N.; Clerici, A.; Punta, C.; Porta, O. Efficient radical domino approach to β-aminoalcohols from arylamines and alcohols triggered by Ti(III)/t-BuOOH. Tetrahedron 2010, 66, 2044-2052.
    • (2010) Tetrahedron , vol.66 , pp. 2044-2052
    • Spaccini, R.1    Ghilardi, A.2    Pastori, N.3    Clerici, A.4    Punta, C.5    Porta, O.6
  • 76
    • 77956200751 scopus 로고    scopus 로고
    • Free-radical addition to ketimines generated in situ. New one-pot synthesis of quaternary α-aminoamides promoted by a H2O2/TiCl4-Zn/HCONH2 System
    • Pastori, N.; Greco, C.; Clerici, A.; Punta, C.; Porta, O. Free-radical addition to ketimines generated in situ. New one-pot synthesis of quaternary α-aminoamides promoted by a H2O2/TiCl4-Zn/HCONH2 System. Org. Lett. 2010, 12, 3898-3901.
    • (2010) Org. Lett. , vol.12 , pp. 3898-3901
    • Pastori, N.1    Greco, C.2    Clerici, A.3    Punta, C.4    Porta, O.5
  • 77
    • 84867888631 scopus 로고    scopus 로고
    • Free-radical hydroxymethylation of ketimines generated in situ: A one-pot multicomponent synthesis of β, β-disubstituted-β-aminoalcohols
    • Rossi, B.; Pastori, N.; Clerici, A.; Punta, C. Free-radical hydroxymethylation of ketimines generated in situ: A one-pot multicomponent synthesis of β, β-disubstituted-β-aminoalcohols. Tetrahedron 2012, 68, 10151-10156.
    • (2012) Tetrahedron , vol.68 , pp. 10151-10156
    • Rossi, B.1    Pastori, N.2    Clerici, A.3    Punta, C.4
  • 78
    • 33646449533 scopus 로고    scopus 로고
    • Free-radical version of the strecker synthesis of α-aminoamides promoted by aqueous H2O2/TiCl3/HCONH2 system
    • Cannella, R.; Clerici, A.; Panzeri, W.; Pastori, N.; Punta, C.; Porta, O. Free-radical version of the strecker synthesis of α-aminoamides promoted by aqueous H2O2/TiCl3/HCONH2 system. J. Am. Chem. Soc. 2006, 128, 5358-5359.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 5358-5359
    • Cannella, R.1    Clerici, A.2    Panzeri, W.3    Pastori, N.4    Punta, C.5    Porta, O.6
  • 79
    • 0032796594 scopus 로고    scopus 로고
    • Diethylzinc mediated radical additions to glyoxylate imines
    • Bertrand, M.P.; Feray, L.; Nouguier, R.; Perfetti, P. Diethylzinc mediated radical additions to glyoxylate imines. Synlett 1999, 7, 1148-1150.
    • (1999) Synlett , vol.7 , pp. 1148-1150
    • Bertrand, M.P.1    Feray, L.2    Nouguier, R.3    Perfetti, P.4
  • 80
    • 0032784299 scopus 로고    scopus 로고
    • Diethylzinc: A chain-transfer agent in intermolecular radical additions. A parallel with triethylborane
    • Bertrand, M.P.; Feray, L.; Nouguier, R.; Perfetti, P. Diethylzinc: A chain-transfer agent in intermolecular radical additions. A parallel with triethylborane. J. Org. Chem. 1999, 64, 9189-9193.
    • (1999) J. Org. Chem. , vol.64 , pp. 9189-9193
    • Bertrand, M.P.1    Feray, L.2    Nouguier, R.3    Perfetti, P.4
  • 81
    • 0141629311 scopus 로고    scopus 로고
    • Initiator-dependent chemoselective addition of THF radical to aldehyde and aldimine and its application to a three-component reaction
    • Yamada, K.; Yamamoto, Y.; Tomioka, K. Initiator-dependent chemoselective addition of THF radical to aldehyde and aldimine and its application to a three-component reaction. Org. Lett. 2003, 5, 1797-1799.
    • (2003) Org. Lett. , vol.5 , pp. 1797-1799
    • Yamada, K.1    Yamamoto, Y.2    Tomioka, K.3
  • 82
    • 9944243162 scopus 로고    scopus 로고
    • Dimethylzinc-initiated radical reaction of cyclic ethers with arylamines, alkoxyamines, and dialkylhydrazines
    • Yamamoto, Y.; Maekawa, M.; Akindele, T.; Yamada, K.; Tomioka, K. Dimethylzinc-initiated radical reaction of cyclic ethers with arylamines, alkoxyamines, and dialkylhydrazines. Tetrahedron 2005, 61, 379-384.
    • (2005) Tetrahedron , vol.61 , pp. 379-384
    • Yamamoto, Y.1    Maekawa, M.2    Akindele, T.3    Yamada, K.4    Tomioka, K.5
  • 83
    • 45449090945 scopus 로고    scopus 로고
    • Conjugate addition reaction of THF-2-yl radical with α, β-unsaturated N-tosyl imines using a dimethylzinc-air initiator
    • Yamada, K.; Umeki, H.; Maekawa, M.; Yamamoto, Y.; Akindele, T.; Nakano, M.; Tomioka, K. Conjugate addition reaction of THF-2-yl radical with α, β-unsaturated N-tosyl imines using a dimethylzinc-air initiator. Tetrahedron 2008, 64, 7258-7265.
    • (2008) Tetrahedron , vol.64 , pp. 7258-7265
    • Yamada, K.1    Umeki, H.2    Maekawa, M.3    Yamamoto, Y.4    Akindele, T.5    Nakano, M.6    Tomioka, K.7
  • 84
    • 4143088241 scopus 로고    scopus 로고
    • Direct aminoalkylation of cycloalkanes through dimethylzinc-initiated radical process
    • Yamada, K.; Yamamoto, Y.; Maekawa, M.; Chen, J.B.; Tomioka, K. Direct aminoalkylation of cycloalkanes through dimethylzinc-initiated radical process. Tetrahedron Lett. 2004, 45, 6595-6597.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 6595-6597
    • Yamada, K.1    Yamamoto, Y.2    Maekawa, M.3    Chen, J.B.4    Tomioka, K.5
  • 85
    • 30944437087 scopus 로고    scopus 로고
    • Tin-free intermolecular addition of primary alkyls to imines via the dimethylzinc-air radical process
    • Yamada, K.; Yamamoto, Y.; Maekawa, M.; Akindele, T.; Umeki, H.; Tomioka, K. Tin-free intermolecular addition of primary alkyls to imines via the dimethylzinc-air radical process. Org. Lett. 2006, 8, 87-89.
    • (2006) Org. Lett. , vol.8 , pp. 87-89
    • Yamada, K.1    Yamamoto, Y.2    Maekawa, M.3    Akindele, T.4    Umeki, H.5    Tomioka, K.6
  • 87
    • 1442299995 scopus 로고    scopus 로고
    • Introduction of functionalized C1, C2, and C3 units to imines through the dimethylzinc-Air-initiated radical addition
    • Yamada, K.I.; Yamamoto, Y.; Maekawa, M.; Tomioka, K. Introduction of functionalized C1, C2, and C3 units to imines through the dimethylzinc-Air-initiated radical addition. J. Org. Chem. 2004, 69, 1531-1534.
    • (2004) J. Org. Chem. , vol.69 , pp. 1531-1534
    • Yamada, K.I.1    Yamamoto, Y.2    Maekawa, M.3    Tomioka, K.4
  • 88
    • 77949822698 scopus 로고    scopus 로고
    • Multicomponent C-alkylation reactions of aromatic aldimines with trialkylboranes reagents
    • Valpuesta, M.; Munoz, C.; Diaz, A.; Torres, G.; Suau, R. Multicomponent C-alkylation reactions of aromatic aldimines with trialkylboranes reagents. Eur. J. Org. Chem. 2010, 1934-1942.
    • (2010) Eur. J. Org. Chem. , pp. 1934-1942
    • Valpuesta, M.1    Munoz, C.2    Diaz, A.3    Torres, G.4    Suau, R.5
  • 89
    • 33644652412 scopus 로고    scopus 로고
    • Reactive ketimino radical acceptors: Intermolecular alkyl radical addition to imines with a phenolic hydroxyl group
    • Miyabe, H.; Yamaoka, Y.; Takemoto, Y. Reactive ketimino radical acceptors: Intermolecular alkyl radical addition to imines with a phenolic hydroxyl group. J. Org. Chem. 2006, 71, 2099-2106.
    • (2006) J. Org. Chem. , vol.71 , pp. 2099-2106
    • Miyabe, H.1    Yamaoka, Y.2    Takemoto, Y.3
  • 90
    • 0032509938 scopus 로고    scopus 로고
    • Carbon-carbon bond formation via intermolecular carbon radical addition to aldoxime ethers
    • Miyabe, H.; Shibata, R.; Ushiro, C.; Naito, T. Carbon-carbon bond formation via intermolecular carbon radical addition to aldoxime ethers. Tetrahedron Lett. 1998, 39, 631-634.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 631-634
    • Miyabe, H.1    Shibata, R.2    Ushiro, C.3    Naito, T.4
  • 91
    • 0032541555 scopus 로고    scopus 로고
    • Intermolecular alkyl radical addition to the carbon-nitrogen double bond of oxime ethers and hydrazones
    • Miyabe, H.; Shibata, R.; Sangawa, M.; Ushiro, C.; Naito, T. Intermolecular alkyl radical addition to the carbon-nitrogen double bond of oxime ethers and hydrazones. Tetrahedron 1998, 54, 11431-11444.
    • (1998) Tetrahedron , vol.54 , pp. 11431-11444
    • Miyabe, H.1    Shibata, R.2    Sangawa, M.3    Ushiro, C.4    Naito, T.5
  • 92
    • 0033543464 scopus 로고    scopus 로고
    • Alkylative amination of aldehydes via carbon-carbon bond formation based on radical addition to carbon-nitrogen double bond
    • Miyabe, H.; Yamakawa, K.; Yoshioka, N.; Naito, T. Alkylative amination of aldehydes via carbon-carbon bond formation based on radical addition to carbon-nitrogen double bond. Tetrahedron 1999, 55, 11209-11218.
    • (1999) Tetrahedron , vol.55 , pp. 11209-11218
    • Miyabe, H.1    Yamakawa, K.2    Yoshioka, N.3    Naito, T.4
  • 93
    • 0037175475 scopus 로고    scopus 로고
    • A concise asymmetric synthesis of 5, 8-disubstituted indolizidine alkaloids. Total synthesis of (-)-indolizidine 209B
    • Song, Y.C.; Okamoto, S.; Sato, F. A concise asymmetric synthesis of 5, 8-disubstituted indolizidine alkaloids. Total synthesis of (-)-indolizidine 209B. Tetrahedron Lett. 2002, 43, 8635-8637.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 8635-8637
    • Song, Y.C.1    Okamoto, S.2    Sato, F.3
  • 94
    • 0001297835 scopus 로고
    • Application of the intramolecular Schmidt reaction to the asymmetric-synthesis of (-)-indolizidine-209b from pulegone
    • Aube, J.; Rafferty, P.S.; Milligan, G.L. Application of the intramolecular Schmidt reaction to the asymmetric-synthesis of (-)-indolizidine-209b from pulegone. Heterocycles 1993, 35, 1141-1147.
    • (1993) Heterocycles , vol.35 , pp. 1141-1147
    • Aube, J.1    Rafferty, P.S.2    Milligan, G.L.3
  • 95
    • 0027292517 scopus 로고
    • A chiral synthesis of (8r, 8as)-hexahydro-8-methyl-5(1h)-indolizinone
    • Satake, A.; Shimizu, I. A chiral synthesis of (8r, 8as)-hexahydro-8-methyl-5(1h)-indolizinone. Tetrahedron: Asymmetry 1993, 4, 1405-1408.
    • (1993) Tetrahedron: Asymmetry , vol.4 , pp. 1405-1408
    • Satake, A.1    Shimizu, I.2
  • 96
    • 37649003075 scopus 로고    scopus 로고
    • Novel synthesis of substituted pyrrolidines and piperidines via radical addition-Ionic cyclization reaction of oxime ethers
    • Miyata, O.; Takahashi, S.; Tamura, A.; Ueda, M.; Naito, T. Novel synthesis of substituted pyrrolidines and piperidines via radical addition-Ionic cyclization reaction of oxime ethers. Tetrahedron 2008, 64, 1270-1284.
    • (2008) Tetrahedron , vol.64 , pp. 1270-1284
    • Miyata, O.1    Takahashi, S.2    Tamura, A.3    Ueda, M.4    Naito, T.5
  • 97
    • 84898032753 scopus 로고    scopus 로고
    • Lewis acid-catalyzed cascade radical addition/cyclization for the synthesis of 3-substituted isoindolin-1-one derivatives
    • Zhang, L.; Kim, J.B.; Jang, D.O. Lewis acid-catalyzed cascade radical addition/cyclization for the synthesis of 3-substituted isoindolin-1-one derivatives. Tetrahedron Lett. 2014, 55, 2654-2658.
    • (2014) Tetrahedron Lett. , vol.55 , pp. 2654-2658
    • Zhang, L.1    Kim, J.B.2    Jang, D.O.3
  • 98
    • 84862575222 scopus 로고    scopus 로고
    • Inter-and intramolecular carbon-carbon bond-forming radical reactions
    • Miyabe, H. Inter- and intramolecular carbon-carbon bond-forming radical reactions. Synlett 2012, 23, 1709-1724.
    • (2012) Synlett , vol.23 , pp. 1709-1724
    • Miyabe, H.1
  • 99
    • 0001342149 scopus 로고    scopus 로고
    • 1, 3-stereoinduction in radical additions to glyoxylate imines
    • Bertrand, M.P.; Feray, L.; Nouguier, R.; Stella, L. 1, 3-stereoinduction in radical additions to glyoxylate imines. Synlett 1998, 7, 780-782.
    • (1998) Synlett , vol.7 , pp. 780-782
    • Bertrand, M.P.1    Feray, L.2    Nouguier, R.3    Stella, L.4
  • 100
    • 0027392328 scopus 로고
    • Asymmetric thermal-reactions with oppolzer camphor sultam
    • Kim, B.H.; Curran, D.P. Asymmetric thermal-reactions with oppolzer camphor sultam. Tetrahedron 1993, 49, 293-318.
    • (1993) Tetrahedron , vol.49 , pp. 293-318
    • Kim, B.H.1    Curran, D.P.2
  • 101
    • 0000227151 scopus 로고    scopus 로고
    • Highly diastereoselective radical addition to oxime ethers: Asymmetric synthesis of beta-amino acids
    • Miyabe, H.; Fujii, K.; Naito, T. Highly diastereoselective radical addition to oxime ethers: Asymmetric synthesis of beta-amino acids. Org. Lett. 1999, 1, 569-572.
    • (1999) Org. Lett. , vol.1 , pp. 569-572
    • Miyabe, H.1    Fujii, K.2    Naito, T.3
  • 102
    • 0042178291 scopus 로고    scopus 로고
    • Radical addition to oxime ethers for asymmetric synthesis of beta-amino acid derivatives
    • Miyabe, H.; Fujii, K.; Naito, T. Radical addition to oxime ethers for asymmetric synthesis of beta-amino acid derivatives. Org. Biomol. Chem. 2003, 1, 381-390.
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 381-390
    • Miyabe, H.1    Fujii, K.2    Naito, T.3
  • 103
    • 0001651037 scopus 로고    scopus 로고
    • Highly stereoselective intermolecular radical addition to aldehyde hydrazones from a chiral 3-amino-2-oxazolidinone
    • Friestad, G.K.; Qin, J. Highly stereoselective intermolecular radical addition to aldehyde hydrazones from a chiral 3-amino-2-oxazolidinone. J. Am. Chem. Soc. 2000, 122, 8329-8330.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 8329-8330
    • Friestad, G.K.1    Qin, J.2
  • 104
    • 0035840955 scopus 로고    scopus 로고
    • Intermolecular alkyl radical addition to chiral N-acylhydrazones mediated by manganese carbonyl
    • Friestad, G.K.; Qin, J. Intermolecular alkyl radical addition to chiral N-acylhydrazones mediated by manganese carbonyl. J. Am. Chem. Soc. 2001, 123, 9922-9923.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 9922-9923
    • Friestad, G.K.1    Qin, J.2
  • 105
    • 4644259363 scopus 로고    scopus 로고
    • Stereoselective Mn-mediated coupling of functionalized iodides and hydrazones: A synthetic entry to the tubulysin gamma-amino acids
    • Friestad, G.K.; Marie, J.C.; Deveau, A.M. Stereoselective Mn-mediated coupling of functionalized iodides and hydrazones: A synthetic entry to the tubulysin gamma-amino acids. Org. Lett. 2004, 6, 3249-3252.
    • (2004) Org. Lett. , vol.6 , pp. 3249-3252
    • Friestad, G.K.1    Marie, J.C.2    Deveau, A.M.3
  • 106
    • 23044488109 scopus 로고    scopus 로고
    • Radical addition approach to asymmetric amine synthesis: Design, implementation, and comparison of chiral N-acylhydrazones
    • Friestad, G.K.; Draghici, C.; Soukri, M.; Qin, J. Radical addition approach to asymmetric amine synthesis: Design, implementation, and comparison of chiral N-acylhydrazones. J. Org. Chem. 2005, 70, 6330-6338.
    • (2005) J. Org. Chem. , vol.70 , pp. 6330-6338
    • Friestad, G.K.1    Draghici, C.2    Soukri, M.3    Qin, J.4
  • 107
    • 33750455795 scopus 로고    scopus 로고
    • Mn-mediated coupling of alkyl iodides and chiral N-acylhydrazones: Optimization, scope, and evidence for a radical mechanism
    • Friestad, G.K.; Marie, J.C.; Suh, Y.S.; Qin, J. Mn-mediated coupling of alkyl iodides and chiral N-acylhydrazones: Optimization, scope, and evidence for a radical mechanism. J. Org. Chem. 2006, 71, 7016-7027.
    • (2006) J. Org. Chem. , vol.71 , pp. 7016-7027
    • Friestad, G.K.1    Marie, J.C.2    Suh, Y.S.3    Qin, J.4
  • 108
    • 35548932985 scopus 로고    scopus 로고
    • Quinine synthesis studies: A radical-ionic annulation via Mn-mediated addition to chiral N-acylhydrazones
    • Korapala, C.S.; Qin, J.; Friestad, G.K. Quinine synthesis studies: A radical-ionic annulation via Mn-mediated addition to chiral N-acylhydrazones. Org. Lett. 2007, 9, 4243-4246.
    • (2007) Org. Lett. , vol.9 , pp. 4243-4246
    • Korapala, C.S.1    Qin, J.2    Friestad, G.K.3
  • 109
    • 55549118290 scopus 로고    scopus 로고
    • Mn-mediated coupling of alkyl iodides and ketimines: A radical addition route to α, α-disubstituted α-aminoesters
    • Friestad, G.K.; Ji, A. Mn-mediated coupling of alkyl iodides and ketimines: A radical addition route to α, α-disubstituted α-aminoesters. Org. Lett. 2008, 10, 2311-2313.
    • (2008) Org. Lett. , vol.10 , pp. 2311-2313
    • Friestad, G.K.1    Ji, A.2
  • 110
    • 64349108309 scopus 로고    scopus 로고
    • Synthesis of γ-amino esters via Mn-mediated radical addition to chiral γ-Hydrazonoesters
    • Friestad, G.K.; Banerjee, K. Synthesis of γ-amino esters via Mn-mediated radical addition to chiral γ-Hydrazonoesters. Org. Lett. 2009, 11, 1095-1098.
    • (2009) Org. Lett. , vol.11 , pp. 1095-1098
    • Friestad, G.K.1    Banerjee, K.2
  • 111
    • 0033966817 scopus 로고    scopus 로고
    • Asymmetric synthesis of alpha-amino acids based on carbon radical addition to glyoxylic oxime ether
    • Miyabe, H.; Ushiro, C.; Ueda, M.; Yamakawa, K.; Naito, T. Asymmetric synthesis of alpha-amino acids based on carbon radical addition to glyoxylic oxime ether. J. Org. Chem. 2000, 65, 176-185.
    • (2000) J. Org. Chem. , vol.65 , pp. 176-185
    • Miyabe, H.1    Ushiro, C.2    Ueda, M.3    Yamakawa, K.4    Naito, T.5
  • 112
    • 0242323495 scopus 로고    scopus 로고
    • Enantioselective radical addition to N-acyl hydrazones mediated by chiral Lewis acids
    • Friestad, G.K.; Shen, Y.H.; Ruggles, E.L. Enantioselective radical addition to N-acyl hydrazones mediated by chiral Lewis acids. Angew. Chem. Int. Ed. 2003, 42, 5061-5063.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 5061-5063
    • Friestad, G.K.1    Shen, Y.H.2    Ruggles, E.L.3
  • 113
    • 84885064334 scopus 로고    scopus 로고
    • The chemistry of amine radical cations produced by visible light photoredox catalysis
    • Hu, J.; Wang, J.; Nguyen, T.H.; Zheng, N. The chemistry of amine radical cations produced by visible light photoredox catalysis. Beilstein J. Org. Chem. 2013, 9, 1977-2001.
    • (2013) Beilstein J. Org. Chem. , vol.9 , pp. 1977-2001
    • Hu, J.1    Wang, J.2    Nguyen, T.H.3    Zheng, N.4
  • 114
    • 0028039862 scopus 로고
    • A new method in radical chemistry-Generation of radicals by photoinduced electron-transfer and fragmentation of the radical-cation
    • Albini, A.; Mella, M.; Freccero, M. A new method in radical chemistry-Generation of radicals by photoinduced electron-transfer and fragmentation of the radical-cation. Tetrahedron 1994, 50, 575-607.
    • (1994) Tetrahedron , vol.50 , pp. 575-607
    • Albini, A.1    Mella, M.2    Freccero, M.3
  • 115
    • 0026667909 scopus 로고
    • Direct carbon-carbon bond formation strategy at α-position of tertiary-amines by photoinduced electron-transfer (PET) processes
    • Pandey, G.; Rani, K.S.; Lakshmaiah, G. Direct carbon-carbon bond formation strategy at α-position of tertiary-amines by photoinduced electron-transfer (PET) processes. Tetrahedron Lett. 1992, 33, 5107-5110.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 5107-5110
    • Pandey, G.1    Rani, K.S.2    Lakshmaiah, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.