메뉴 건너뛰기




Volumn 134, Issue 22, 2012, Pages 9102-9105

Catalytic asymmetric synthesis of secondary nitriles via stereoconvergent negishi arylations and alkenylations of racemic α-bromonitriles

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL BROMIDES; ALKYL SUBSTITUENT; ARYL NITRILE; ARYLATIONS; ARYLZINC REAGENTS; ASYMMETRIC SYNTHESIS; CARBON-CARBON BOND FORMATION; CROSS-COUPLINGS; ELECTROPHILES; ENANTIOSELECTIVE; ENANTIOSELECTIVE SYNTHESIS; LOW TEMPERATURES; NEGISHI REACTIONS; OXAZOLINES;

EID: 84861902827     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja303442q     Document Type: Article
Times cited : (145)

References (36)
  • 3
    • 33746470627 scopus 로고    scopus 로고
    • For leading references, see: Georg Thieme Verlag: Stuttgart, Germany
    • For leading references, see: Science of Synthesis; Murahashi, S.-I., Ed.; Georg Thieme Verlag: Stuttgart, Germany, 2004; Vol. 19.
    • (2004) Science of Synthesis , vol.19
    • Murahashi, S.-I.1
  • 6
    • 0004219524 scopus 로고    scopus 로고
    • Collins, A. N. Sheldrake, G. N. Crosby, J. John Wiley & Sons: New York, Chapter 15
    • Casalnuovo, A. L.; Rajanbabu, T. V. In Chirality in Industry II; Collins, A. N.; Sheldrake, G. N.; Crosby, J., Eds.; John Wiley & Sons: New York, 1997; Chapter 15.
    • (1997) Chirality in Industry II
    • Casalnuovo, A.L.1    Rajanbabu, T.V.2
  • 7
    • 84861841500 scopus 로고    scopus 로고
    • De Vries, J. G. Molander, G. A. Evans, P. A. Georg Thieme Verlag: Stuttgart, Germany
    • van Leeuwen, P. W. N. In Science of Synthesis, Stereoselective Synthesis; De Vries, J. G.; Molander, G. A.; Evans, P. A., Eds.; Georg Thieme Verlag: Stuttgart, Germany, 2011; Vol. 1, pp 409-475.
    • (2011) Science of Synthesis, Stereoselective Synthesis , vol.1 , pp. 409-475
    • Van Leeuwen, P.W.N.1
  • 8
    • 0000176028 scopus 로고    scopus 로고
    • Jacobsen, E. N. Pfaltz, A. Yamamoto, H. Springer: New York
    • RajanBabu, T. V.; Casalnuovo, A. L. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: New York, 1999; Vol. 1, pp 267-378.
    • (1999) Comprehensive Asymmetric Catalysis , vol.1 , pp. 267-378
    • Rajanbabu, T.V.1    Casalnuovo, A.L.2
  • 15
    • 77950417415 scopus 로고    scopus 로고
    • Suzuki reactions
    • Suzuki reactions: He, A.; Falck, J. R. J. Am. Chem. Soc. 2010, 132, 2524-2525
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 2524-2525
    • He, A.1    Falck, J.R.2
  • 18
    • 16844363000 scopus 로고    scopus 로고
    • Alkylations of α-haloamides
    • Alkylations of α-haloamides: Fischer, C.; Fu, G. C. J. Am. Chem. Soc. 2005, 127, 4594-4595
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 4594-4595
    • Fischer, C.1    Fu, G.C.2
  • 19
    • 23044496800 scopus 로고    scopus 로고
    • Alkylations of benzylic halides
    • Alkylations of benzylic halides: Arp, F. O.; Fu, G. C. J. Am. Chem. Soc. 2005, 127, 10482-10483
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 10482-10483
    • Arp, F.O.1    Fu, G.C.2
  • 20
    • 40949123444 scopus 로고    scopus 로고
    • Alkylations of allylic halides
    • Alkylations of allylic halides: Son, S.; Fu, G. C. J. Am. Chem. Soc. 2008, 130, 2756-2757
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 2756-2757
    • Son, S.1    Fu, G.C.2
  • 21
    • 52449132069 scopus 로고    scopus 로고
    • Arylations of propargylic halides and carbonates
    • Arylations of propargylic halides and carbonates: Smith, S. W.; Fu, G. C. J. Am. Chem. Soc. 2008, 130, 12645-12647
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 12645-12647
    • Smith, S.W.1    Fu, G.C.2
  • 24
    • 84856021728 scopus 로고    scopus 로고
    • For a very recent application of our asymmetric allylation method in the total synthesis of a natural product (carolacton), see
    • For a very recent application of our asymmetric allylation method in the total synthesis of a natural product (carolacton), see: Schmidt, T.; Kischning, A. Angew. Chem., Int. Ed. 2012, 51, 1063-1066
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 1063-1066
    • Schmidt, T.1    Kischning, A.2
  • 26
    • 77950503735 scopus 로고    scopus 로고
    • For enantioselective Kumada reactions of α-haloketones that proceed at -60 °C, see
    • For enantioselective Kumada reactions of α-haloketones that proceed at -60 °C, see: Lou, S.; Fu, G. C. J. Am. Chem. Soc. 2010, 132, 1264-1266
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 1264-1266
    • Lou, S.1    Fu, G.C.2
  • 29
    • 1042288193 scopus 로고    scopus 로고
    • For early suggestions, see
    • For early suggestions, see: Zhou, J.; Fu, G. C. J. Am. Chem. Soc. 2004, 126, 1340-1341
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 1340-1341
    • Zhou, J.1    Fu, G.C.2
  • 31
    • 80053339478 scopus 로고    scopus 로고
    • For a recent discussion and leading references, see
    • For a recent discussion and leading references, see: Zultanski, S. L.; Fu, G. C. J. Am. Chem. Soc. 2011, 133, 15362-15364
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 15362-15364
    • Zultanski, S.L.1    Fu, G.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.