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Volumn 61, Issue 39, 2005, Pages 9319-9324

Deallyloxy- and debenzyloxycarbonylation of protected alcohols, amines and thiols via a naphthalene-catalysed lithiation reaction

Author keywords

Alcohols; Allyloxycarbonyl; Amines; Benzyloxycarbonyl; Deprotection; Lithium; Naphthalene; Thiols

Indexed keywords

ALCOHOL DERIVATIVE; AMINE; AMMONIA; CARBON; CARBONIC ACID; INORGANIC COMPOUND; METHANOL; NAPHTHALENE; THIOL DERIVATIVE;

EID: 23944431622     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.07.055     Document Type: Article
Times cited : (21)

References (61)
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    • For a polymer-supported version of this reaction, see: (a) C. Gómez, S. Ruiz, and M. Yus Tetrahedron Lett. 39 1998 1397 1400
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    • We have reported that geranyllithium can be generated from a geranyl carbonate by a naphthalene-catalysed lithiation at 0°C: see Ref. 16.
    • We have reported that geranyllithium can be generated from a geranyl carbonate by a naphthalene-catalysed lithiation at 0°C: see Ref. 16.
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    • see Ref. 15a.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.