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Volumn 63, Issue 48, 2007, Pages 11998-12006

Ion pairing effects on the regioselectivity of arylic versus benzylic C-O bond reductive cleavage: synthetic applications

Author keywords

Alkali metals; Cleavage reactions; Ionic pairs; Metallation; Natural products; Regioselectivity

Indexed keywords

1 (3,4,5 TRIMETHOXYPHENYL) 2 ETHANE; 1 [2 (ETHOXYMETHOXY) 3 METHOXYPHENYL] 2 (3,4,5 TRIMETHOXYPHENYL)ETHANOL; 1 [3 (ETHOXYMETHOXY) 4 METHOXYPHENYL] 2 (3,4,5 TRIMETHOXYPHENYL)ETHANOL; 1 PHENYL 2 (3,4,5 TRIMETHOXYPHENYL)ETHANOL; 1,3 DIMETHOXY 2 BUTYL 5 METHOXYMETHYLBENZENE; 1,3 DIMETHOXY 2 HEXYL 5 METHOXYMETHYLBENZENE; 1,3 DIMETHOXY 2,5 DIALKYLBENZENE; 2,6 DIMETHOXY 4 METHOXYMETHYLBENZOIC ACID METHYL ESTER; 3,4,5 TRIMETHOXYBENZYL METHYL ETHER; 5 [1 HYDROXY 2 (3,4,5 TRIMETHOXYPHENYL)ETHYL] 2 METHOXYPHENOL; 5 [1 METHOXY 2 (3,4,5 TRIMETHOXYPHENYL)ETHYL] 2 METHOXYPHENOL; ALKALI METAL; BENZENE DERIVATIVE; BENZILIC ACID; BIS (2,6 DIMETHOXY 4 METHOXYMETHYLPHENYL)METHANOL; CARBON; COMBRETASTATIN; COMBRETASTATIN A4; ION; ISOCOMBRETASTATIN A; LITHIUM; OXYGEN; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; RESORCINOL DERIVATIVE; SODIUM; UNCLASSIFIED DRUG;

EID: 35348866727     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.09.010     Document Type: Article
Times cited : (15)

References (39)
  • 1
    • 14844291428 scopus 로고    scopus 로고
    • For a recent collection of papers on this topic, see: Tetrahedron, Symposium-in-Print no. 111. Guest Eds.
    • For a recent collection of papers on this topic, see: Tetrahedron, Symposium-in-Print no. 111. Najera C., and Yus M. Guest Eds. Tetrahedron 61 (2005) 3139-3450
    • (2005) Tetrahedron , vol.61 , pp. 3139-3450
    • Najera, C.1    Yus, M.2
  • 3
    • 0032191029 scopus 로고    scopus 로고
    • and references cited therein
    • Azzena U., Pilo L., and Sechi A. Tetrahedron 54 (1998) 12389-12398 and references cited therein
    • (1998) Tetrahedron , vol.54 , pp. 12389-12398
    • Azzena, U.1    Pilo, L.2    Sechi, A.3
  • 4
  • 21
    • 35348917930 scopus 로고    scopus 로고
    • note
    • 3 (0.45 equiv), led to the formation of bis-(2,6-dimethoxy-4-methoxymethylphenyl)methanol, 2e, in 55% isolated yield. See Section 4.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.