메뉴 건너뛰기




Volumn 345, Issue 3, 2003, Pages 353-355

Synthesis of Functionalised Phenylalanines Using Rhodium Catalysis in Water

Author keywords

Arylation; Boronic acids; C C coupling; Conjugate addition; Rhodium

Indexed keywords

BORONIC ACID DERIVATIVE; PHENYLALANINE DERIVATIVE; RHODIUM; WATER;

EID: 0041409946     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/adsc.200390039     Document Type: Article
Times cited : (34)

References (33)
  • 1
    • 0000573602 scopus 로고
    • [1] M. North, Contemp. Org. Synth. 1995, 2, 269; R. Williams, Synthesis of Optically Active α-Amino Acids, Pergamon Press, Oxford, 1989; G.C. Barrett (Ed.), Chemistry and Biochemistry of the Amino Acids, Chapman & Hall, London, 1985.
    • (1995) Contemp. Org. Synth. , vol.2 , pp. 269
    • North, M.1
  • 2
    • 0000573602 scopus 로고
    • Pergamon Press, Oxford
    • M. North, Contemp. Org. Synth. 1995, 2, 269; R. Williams, Synthesis of Optically Active α-Amino Acids, Pergamon Press, Oxford, 1989; G.C. Barrett (Ed.), Chemistry and Biochemistry of the Amino Acids, Chapman & Hall, London, 1985.
    • (1989) Synthesis of Optically Active α-Amino Acids
    • Williams, R.1
  • 3
    • 0000573602 scopus 로고
    • Chapman & Hall, London
    • M. North, Contemp. Org. Synth. 1995, 2, 269; R. Williams, Synthesis of Optically Active α-Amino Acids, Pergamon Press, Oxford, 1989; G.C. Barrett (Ed.), Chemistry and Biochemistry of the Amino Acids, Chapman & Hall, London, 1985.
    • (1985) Chemistry and Biochemistry of the Amino Acids
    • Barrett, G.C.1
  • 4
    • 0004005454 scopus 로고
    • (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Georg Thieme Verlag, Stuttgart
    • [2] H. Kunz, Stereoselective Synthesis, (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Georg Thieme Verlag, Stuttgart, 1995; N. A. Petasis, I. A. Zavialov J. Am. Chem. Soc. 1997, 119, 445; N. A. Petasis, I. A. Zavialov J. Am. Chem. Soc. 1998, 120, 11798; M. J. O'Donnell, W. D. Bennett, Tetrahedron 1988, 44, 5489.
    • (1995) Stereoselective Synthesis
    • Kunz, H.1
  • 5
    • 0031055591 scopus 로고    scopus 로고
    • H. Kunz, Stereoselective Synthesis, (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Georg Thieme Verlag, Stuttgart, 1995; N. A. Petasis, I. A. Zavialov J. Am. Chem. Soc. 1997, 119, 445; N. A. Petasis, I. A. Zavialov J. Am. Chem. Soc. 1998, 120, 11798; M. J. O'Donnell, W. D. Bennett, Tetrahedron 1988, 44, 5489.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 445
    • Petasis, N.A.1    Zavialov, I.A.2
  • 6
    • 0032544945 scopus 로고    scopus 로고
    • H. Kunz, Stereoselective Synthesis, (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Georg Thieme Verlag, Stuttgart, 1995; N. A. Petasis, I. A. Zavialov J. Am. Chem. Soc. 1997, 119, 445; N. A. Petasis, I. A. Zavialov J. Am. Chem. Soc. 1998, 120, 11798; M. J. O'Donnell, W. D. Bennett, Tetrahedron 1988, 44, 5489.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 11798
    • Petasis, N.A.1    Zavialov, I.A.2
  • 7
    • 0000210412 scopus 로고
    • H. Kunz, Stereoselective Synthesis, (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Georg Thieme Verlag, Stuttgart, 1995; N. A. Petasis, I. A. Zavialov J. Am. Chem. Soc. 1997, 119, 445; N. A. Petasis, I. A. Zavialov J. Am. Chem. Soc. 1998, 120, 11798; M. J. O'Donnell, W. D. Bennett, Tetrahedron 1988, 44, 5489.
    • (1988) Tetrahedron , vol.44 , pp. 5489
    • O'Donnell, M.J.1    Bennett, W.D.2
  • 9
    • 0031768472 scopus 로고    scopus 로고
    • [4] M. J. Burk, Chemtracts: Org. Chem. 1998, 11, 787; R. Noyori, Asymmetric Catalysis in Organic Synthesis, Wiley-Interscience, New York, 1994; Catalytic Asymmetric Synthesis, VCH Publishers, Weinheim, 1993.
    • (1998) Chemtracts: Org. Chem. , vol.11 , pp. 787
    • Burk, M.J.1
  • 10
    • 0031768472 scopus 로고    scopus 로고
    • Wiley-Interscience, New York
    • M. J. Burk, Chemtracts: Org. Chem. 1998, 11, 787; R. Noyori, Asymmetric Catalysis in Organic Synthesis, Wiley-Interscience, New York, 1994; Catalytic Asymmetric Synthesis, VCH Publishers, Weinheim, 1993.
    • (1994) Asymmetric Catalysis in Organic Synthesis
    • Noyori, R.1
  • 11
    • 0031768472 scopus 로고    scopus 로고
    • VCH Publishers, Weinheim
    • M. J. Burk, Chemtracts: Org. Chem. 1998, 11, 787; R. Noyori, Asymmetric Catalysis in Organic Synthesis, Wiley-Interscience, New York, 1994; Catalytic Asymmetric Synthesis, VCH Publishers, Weinheim, 1993.
    • (1993) Catalytic Asymmetric Synthesis
  • 16
    • 5244346814 scopus 로고    scopus 로고
    • [9] M. Sakai, H. Hayashi, N. Miyaura, Organometallics 1997, 16, 4229; Y. Takaya, M. Osgawara, T. Hayashi, M. Sakai, N. Miyaura, J. Am. Chem. Soc. 1998, 120, 5579; S. Sakuma, M. Sakai, R. Itooka, N. Miyaura, J. Org. Chem. 2000, 65, 5951;
    • (1997) Organometallics , vol.16 , pp. 4229
    • Sakai, M.1    Hayashi, H.2    Miyaura, N.3
  • 18
    • 0034703410 scopus 로고    scopus 로고
    • M. Sakai, H. Hayashi, N. Miyaura, Organometallics 1997, 16, 4229; Y. Takaya, M. Osgawara, T. Hayashi, M. Sakai, N. Miyaura, J. Am. Chem. Soc. 1998, 120, 5579; S. Sakuma, M. Sakai, R. Itooka, N. Miyaura, J. Org. Chem. 2000, 65, 5951;
    • (2000) J. Org. Chem. , vol.65 , pp. 5951
    • Sakuma, S.1    Sakai, M.2    Itooka, R.3    Miyaura, N.4
  • 21
    • 0032542313 scopus 로고    scopus 로고
    • [11] M. Sakai, M. Ueda, N. Miyaura, Angew. Chem. Int. Ed. 1998, 37, 3279; M. Ueda, N. Miyaura, J. Org. Chem. 2000, 65, 4450; A. Fürstner, H. Krause, Adv. Synth. Catal. 2001, 343, 343; C. Moreau, C. Hague, A. S. Weller, C. G. Frost, Tetrahedron Lett. 2001, 42, 6957.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 3279
    • Sakai, M.1    Ueda, M.2    Miyaura, N.3
  • 22
    • 0034647925 scopus 로고    scopus 로고
    • M. Sakai, M. Ueda, N. Miyaura, Angew. Chem. Int. Ed. 1998, 37, 3279; M. Ueda, N. Miyaura, J. Org. Chem. 2000, 65, 4450; A. Fürstner, H. Krause, Adv. Synth. Catal. 2001, 343, 343; C. Moreau, C. Hague, A. S. Weller, C. G. Frost, Tetrahedron Lett. 2001, 42, 6957.
    • (2000) J. Org. Chem. , vol.65 , pp. 4450
    • Ueda, M.1    Miyaura, N.2
  • 23
    • 0037984985 scopus 로고    scopus 로고
    • M. Sakai, M. Ueda, N. Miyaura, Angew. Chem. Int. Ed. 1998, 37, 3279; M. Ueda, N. Miyaura, J. Org. Chem. 2000, 65, 4450; A. Fürstner, H. Krause, Adv. Synth. Catal. 2001, 343, 343; C. Moreau, C. Hague, A. S. Weller, C. G. Frost, Tetrahedron Lett. 2001, 42, 6957.
    • (2001) Adv. Synth. Catal. , vol.343 , pp. 343
    • Fürstner, A.1    Krause, H.2
  • 24
    • 0035944181 scopus 로고    scopus 로고
    • M. Sakai, M. Ueda, N. Miyaura, Angew. Chem. Int. Ed. 1998, 37, 3279; M. Ueda, N. Miyaura, J. Org. Chem. 2000, 65, 4450; A. Fürstner, H. Krause, Adv. Synth. Catal. 2001, 343, 343; C. Moreau, C. Hague, A. S. Weller, C. G. Frost, Tetrahedron Lett. 2001, 42, 6957.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 6957
    • Moreau, C.1    Hague, C.2    Weller, A.S.3    Frost, C.G.4
  • 27
    • 0035929982 scopus 로고    scopus 로고
    • C. G. Frost, K. J. Wadsworth Chem. Commun. 2001, 2316; K. Oguma, M. Miura, T. Satoh, M. Nomura J. Organomet. Chem. 2002, 648, 297; L. J. Gooßen, K. Ghosh, Angew. Chem. 2001, 113, 3566.
    • (2001) Chem. Commun. , pp. 2316
    • Frost, C.G.1    Wadsworth, K.J.2
  • 28
    • 0036533201 scopus 로고    scopus 로고
    • C. G. Frost, K. J. Wadsworth Chem. Commun. 2001, 2316; K. Oguma, M. Miura, T. Satoh, M. Nomura J. Organomet. Chem. 2002, 648, 297; L. J. Gooßen, K. Ghosh, Angew. Chem. 2001, 113, 3566.
    • (2002) J. Organomet. Chem. , vol.648 , pp. 297
    • Oguma, K.1    Miura, M.2    Satoh, T.3    Nomura, M.4
  • 29
    • 4243728992 scopus 로고    scopus 로고
    • C. G. Frost, K. J. Wadsworth Chem. Commun. 2001, 2316; K. Oguma, M. Miura, T. Satoh, M. Nomura J. Organomet. Chem. 2002, 648, 297; L. J. Gooßen, K. Ghosh, Angew. Chem. 2001, 113, 3566.
    • (2001) Angew. Chem. , vol.113 , pp. 3566
    • Gooßen, L.J.1    Ghosh, K.2
  • 31
    • 0030878922 scopus 로고    scopus 로고
    • These are commercially available or prepared by established methods; B. M. Trost, G. R. Dake, J. Am. Chem. Soc. 1997, 119, 7595.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 7595
    • Trost, B.M.1    Dake, G.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.