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Volumn 47, Issue 10, 1999, Pages 1380-1383

Synthesis of (R)-(-)-3-methoxymethyl-3-propyl-3,4-dihydrocoumarin from a chiral Michael adduct: Absolute configurations of the allylated products of enantioselective radical-mediated reactions

Author keywords

3 methoxymethyl 3 propyldihydrocoumarin; Absolute configuration; Aldol reaction; Baeyer Villiger reaction

Indexed keywords

COUMARIN DERIVATIVE; INDANONE DERIVATIVE; RADICAL;

EID: 0032753886     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.47.1380     Document Type: Article
Times cited : (6)

References (42)
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    • note
    • 578 + 313° (c=2.0, benzene)} by the cyclization of (S)-3 under basic conditions (using NaOMe) followed by fractional recrystallization.
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    • note
    • For reports of the rate of the Baeyer-Villiger reaction, see: refs 7a and b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.