메뉴 건너뛰기




Volumn 45, Issue 9, 2006, Pages 1469-1473

A highly regioselective salt-free iron-catalyzed allylic alkylation

Author keywords

Alkylation; Carboxylic acids; Iron; Nucleophiles; Regioselectivity

Indexed keywords

NUCLEOPHILES; REGIOSELECTIVITY;

EID: 33746214644     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200503274     Document Type: Article
Times cited : (146)

References (37)
  • 2
    • 0003445429 scopus 로고    scopus 로고
    • (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin
    • b) Comprehensive Asymmetric Catalysis I-III (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, 1999.
    • (1999) Comprehensive Asymmetric Catalysis I-III
  • 3
    • 20444365340 scopus 로고    scopus 로고
    • For a review on iron-catalyzed cross-coupling, see: A. Fürstner, R. Martin, Chem. Lett. 2005, 34, 624.
    • (2005) Chem. Lett. , vol.34 , pp. 624
    • Fürstner, A.1    Martin, R.2
  • 20
    • 2542458288 scopus 로고    scopus 로고
    • The use of ligands sometimes leads to a shift in the regioisomer ratio towards the branched products; for example, see: J. W. Fuller, J. C. Wilt, J. Parr, Org. Lett. 2004, 6, 1301.
    • (2004) Org. Lett. , vol.6 , pp. 1301
    • Fuller, J.W.1    Wilt, J.C.2    Parr, J.3
  • 21
    • 33746248112 scopus 로고    scopus 로고
    • note
    • The character of the metal influences the regiochemical course of allylic alkylations. Ruthenium, molybdenum, rhodium, tungsten, and iridium catalysts often lead to the formation of the branched product, regardless of the substitution pattern of the starting material.
  • 31
    • 10044237251 scopus 로고    scopus 로고
    • For an interesting Fe-catalyzed allylic alkylation of allyl halides, see: R. Martin, A. Fürstner, Angew. Chem. 2004, 116, 4045;
    • (2004) Angew. Chem. , vol.116 , pp. 4045
    • Martin, R.1    Fürstner, A.2
  • 33
    • 33746232314 scopus 로고    scopus 로고
    • patent pending (102005040752.8)
    • B. Plietker, patent pending (102005040752.8)
    • Plietker, B.1
  • 35
    • 33746204441 scopus 로고    scopus 로고
    • note
    • [21]
  • 36
    • 33746232319 scopus 로고    scopus 로고
    • note
    • [13a]
  • 37
    • 33746248108 scopus 로고    scopus 로고
    • note
    • The presented mechanism, including the molecular structures, represents a model. Detailed spectroscopic investigations on the structure of the active catalyst as well as on reactive intermediates are currently underway in our laboratories.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.