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Volumn , Issue 18, 2005, Pages 3095-3102

Bis(chloromethyl) sulfone and sulfoxide as precursors of the corresponding α,α′-dianionic synthons by a chlorine-lithium exchange

Author keywords

Chloro lithium exchange; Dimethyl sulfone dianion; Dimethyl sulfoxide dianion; DTBB catalyzed lithiation

Indexed keywords

HYDROLYSIS; NEGATIVE IONS; SULFUR COMPOUNDS; SYNTHESIS (CHEMICAL); TEMPERATURE DISTRIBUTION;

EID: 28344434833     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-918410     Document Type: Article
Times cited : (2)

References (47)
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    • (f) Yus, M. In The Chemistry of Organolithium Compounds, Vol. 1, Part 2; Rappoport, Z.; Marek, I., Eds.; J. Wiley & Sons: Chichester, 2004, Chap. 11.
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    • note
    • The single chlorine-lithium exchange (for instance a stoichiometric amount of Li) failed, giving a complex mixture of reaction products.
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    • note
    • Under Barbier conditions not many electrophiles are compatible with the strongly reducing reaction mixture carbonyl compounds being appropriate for that purpose.
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    • (g) See also Functionalised Organolithium Compounds, In Tetrahedron Symposium in Print; Nájera, C., Yus, M., Eds.; Tetrahedron 2005, 61 (13), 3125-3450.
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    • and references cited therein
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.