메뉴 건너뛰기




Volumn 14, Issue 12, 2012, Pages 2940-2943

Manganese(III) acetate mediated oxidative radical cyclizations. Toward vicinal all-carbon quaternary stereocenters

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID DERIVATIVE; CARBON; FREE RADICAL; MANGANESE(III) ACETATE DIHYDRATE; ORGANOMETALLIC COMPOUND;

EID: 84862572457     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol300625u     Document Type: Article
Times cited : (49)

References (69)
  • 37
    • 77950844004 scopus 로고    scopus 로고
    • For a recent example of the direct generation of vicinal all-carbon quaternary centers by reaction of a Grignard reagent with an α-chlorotosylhydrazone, see
    • For a recent example of the direct generation of vicinal all-carbon quaternary centers by reaction of a Grignard reagent with an α-chlorotosylhydrazone, see: Hatcher, J. M.; Coltart, D. M. J. Am. Chem. Soc. 2010, 132, 4546-4547
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 4546-4547
    • Hatcher, J.M.1    Coltart, D.M.2
  • 54
    • 70449725405 scopus 로고    scopus 로고
    • For a review of the mechanisms of manganese(III) acetate mediated reactions, see
    • For a review of the mechanisms of manganese(III) acetate mediated reactions, see: Snider, B. B. Tetrahedron 2009, 65, 10738-10744
    • (2009) Tetrahedron , vol.65 , pp. 10738-10744
    • Snider, B.B.1
  • 67
    • 84862515835 scopus 로고    scopus 로고
    • For full experimental details, see SI (CIF); crystallographic data (excluding structure factors) have been deposited with the Cambridge Crystallographic Data Centre (CCDC 879276 and 879277) and can be obtained via.
    • For full experimental details, see SI (CIF); crystallographic data (excluding structure factors) have been deposited with the Cambridge Crystallographic Data Centre (CCDC 879276 and 879277) and can be obtained via http://www.ccdc.cam.ac.uk/data-request/cif.
  • 69
    • 0001713670 scopus 로고
    • For a related ionic iodocarbocylization and lactonization to give a compound with adjacent all-carbon quaternary centers, see
    • For a related ionic iodocarbocylization and lactonization to give a compound with adjacent all-carbon quaternary centers, see: Kitagawa, O.; Inoue, T.; Hirano, K.; Taguchi, T. J. Org. Chem. 1993, 58, 3106-3112
    • (1993) J. Org. Chem. , vol.58 , pp. 3106-3112
    • Kitagawa, O.1    Inoue, T.2    Hirano, K.3    Taguchi, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.