메뉴 건너뛰기




Volumn 17, Issue 44, 2011, Pages 12272-12275

Brønsted acid catalyzed α-alkylation of aldehydes with diaryl methyl alcohols

Author keywords

alcohols; aldehydes; alkylation; Br nsted acid; carbocations

Indexed keywords

ALCOHOL DEHYDRATION; CARBOCATIONS; ENAMINES; ENOLIZATION; METHYL ALCOHOLS;

EID: 80054730818     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201102623     Document Type: Article
Times cited : (21)

References (52)
  • 1
    • 32844457119 scopus 로고    scopus 로고
    • For recent reviews on enamine catalysis, see: B. List, Chem. Commun. 2006, 819-824
    • (2006) Chem. Commun. , pp. 819-824
    • List, B.1
  • 4
    • 53549121402 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 6138-6171
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 6138-6171
  • 9
    • 54749100733 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 7539-7542
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 7539-7542
  • 11
    • 79954434438 scopus 로고    scopus 로고
    • for related aldehyde alkylation via SOMO activation and photo-redox organocatalysis, see
    • E. Gõmez-Bengoa, A. Landa, A. Lizarraga, A. Mielgo, M. Oiarbide, C. Palomo, Chem. Sci. 2011, 2, 353-357; for related aldehyde alkylation via SOMO activation and photo-redox organocatalysis, see
    • (2011) Chem. Sci. , vol.2 , pp. 353-357
    • Gõmez-Bengoa, E.1    Landa, A.2    Lizarraga, A.3    Mielgo, A.4    Oiarbide, M.5    Palomo, C.6
  • 18
    • 55249108726 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 8707-8710.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 8707-8710
  • 19
    • 60149087667 scopus 로고    scopus 로고
    • For diaryl alcohols, see: P. G. Cozzi, L. Zoli, Angew. Chem. 2008, 120, 4230-4234
    • (2008) Angew. Chem. , vol.120 , pp. 4230-4234
    • Cozzi, P.G.1    Zoli, L.2
  • 20
    • 53549118306 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 4162-4166
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4162-4166
  • 22
    • 60149108649 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 1313-1316
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 1313-1316
  • 28
    • 78650090073 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 9685-9688
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 9685-9688
  • 35
    • 38349189109 scopus 로고    scopus 로고
    • for Brønsted acid catalyzed nucleophilic addition to alcohols, see
    • T. Akiyama, Chem. Rev. 2007, 107, 5744-5758; for Brønsted acid catalyzed nucleophilic addition to alcohols, see
    • (2007) Chem. Rev. , vol.107 , pp. 5744-5758
    • Akiyama, T.1
  • 39
    • 37049143497 scopus 로고
    • See the Supporting Information for details.: For examples of ether self-redox reactions, see: M. P. Balfe, J. Kenyon, E. M. Thain, J. Chem. Soc. 1952, 790-796
    • (1952) J. Chem. Soc. , pp. 790-796
    • Balfe, M.P.1    Kenyon, J.2    Thain, E.M.3
  • 41
    • 0001578050 scopus 로고
    • The feasable and rather complicated radical reactions of the ether-derived diaryl cation intermediates can also lead to unproductive consumption of the alchol substrates; for relavent studies, see: C. Y. Choi, L. M. Stock, J. Org. Chem. 1984, 49, 2871-2875
    • (1984) J. Org. Chem. , vol.49 , pp. 2871-2875
    • Choi, C.Y.1    Stock, L.M.2
  • 43
    • 33750613873 scopus 로고    scopus 로고
    • For allylic alkylation of aldehydes through enamine catalysis and metal catalysis, see: I. Ibrahem, A. Cõrdova, Angew. Chem. 2006, 118, 1986-1990
    • (2006) Angew. Chem. , vol.118 , pp. 1986-1990
    • Ibrahem, I.1    Cõrdova, A.2
  • 44
    • 33646573235 scopus 로고    scopus 로고
    • for allylic alkylation of aldehydes through enamine catalysis and Brønsted acid catalysis, see
    • Angew. Chem. Int. Ed. 2006, 45, 1952-1956; for allylic alkylation of aldehydes through enamine catalysis and Brønsted acid catalysis, see
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 1952-1956


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.