메뉴 건너뛰기




Volumn 5, Issue 6, 2010, Pages 1487-1493

Silver-catalyzed benzylation and allylation of tertiary alkyl bromides with organozinc reagents

Author keywords

Alkyl halides; Allylation; Benzylation; Organozinc reagents; Silver

Indexed keywords

ALKYL BROMIDES; ALKYL HALIDES; ALLYLATIONS; BENZYLATION; BENZYLIC; GRIGNARD REAGENT; ORGANOZINC REAGENTS; QUATERNARY CARBON; SILVER SALTS; ZINC REAGENTS;

EID: 77952928037     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201000068     Document Type: Article
Times cited : (30)

References (69)
  • 1
    • 0003422627 scopus 로고    scopus 로고
    • A quaternary carbon center is defined as a carbon atom bonded to four other carbon atoms with single bonds, 6th ed. (Ed.: S. P. Parker), McGraw-Hill, New York
    • A quaternary carbon center is defined as a carbon atom bonded to four other carbon atoms with single bonds: McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed. (Ed.: S. P. Parker), McGraw-Hill, New York, 2003.
    • (2003) McGraw-Hill Dictionary of Scientific and Technical Terms
  • 4
    • 0001521888 scopus 로고
    • c) K. Fuji, Chem. Rev. 1993, 93, 2037-2066;
    • (1993) Chem. Rev. , vol.93 , pp. 2037-2066
    • Fuji, K.1
  • 20
    • 0037021014 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 4137-4139;
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 4137-4139
  • 29
    • 0036643488 scopus 로고    scopus 로고
    • Silver-catalyzed reactions of alkyl halides with organometallic reagents reported by other groups: a) J. K. Kochi, J. Organomet Chem. 2002, 653, 11-19;
    • (2002) J. Organomet Chem. , vol.653 , pp. 11-19
    • Kochi, J.K.1
  • 35
    • 0030964143 scopus 로고    scopus 로고
    • Copper-catalyzed reactions of secondary and tertiary alkyl halides with organometallic reagents reported by other groups: D. H. Burns, J. D. Miller, H. K. Chan, M. O. Delaney, J. Am. Chem. Soc. 1997, 119, 2125-2133.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 2125-2133
    • Burns, D.H.1    Miller, J.D.2    Chan, H.K.3    Delaney, M.O.4
  • 37
    • 77952906730 scopus 로고    scopus 로고
    • Ed.: S. I. Warriner, Thieme, Stuttgart, Chapter 29.2
    • G. J. Rowlands in Science of Synthesis (Houben-Weyl), Vol. 29 (Ed.: S. I. Warriner), Thieme, Stuttgart, 2007, Chapter 29.2.
    • (2007) Science of Synthesis Houben-Weyl , vol.29
    • Rowlands, G.J.1
  • 38
    • 77952906419 scopus 로고    scopus 로고
    • note
    • The plausible by-products are the following: [Figure presented]
  • 46
    • 53549103314 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 5833-5835.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 5833-5835
  • 48
    • 0037021014 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 4137-4139;
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 4137-4139
  • 67
    • 0034678766 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 1462-1464.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 1462-1464


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.