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Volumn 17, Issue 49, 2011, Pages 13877-13882

Preparation of diastereomerically pure dilignol model compounds

Author keywords

diastereoselectivity; hydrides; lignin derivatives; organic chemistry; reduction

Indexed keywords

ARYLOXY; DIASTEREO-SELECTIVITY; DIASTEREOISOMERS; ENOLATES; ERYTHRO; HIGH YIELD; HYDROXY ESTERS; LIGNIN DERIVATIVES; MODEL COMPOUND; ORGANIC CHEMISTRY; TARGET COMPOUND;

EID: 82455205835     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201101579     Document Type: Article
Times cited : (38)

References (45)
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  • 8
    • 34948904441 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 7184-7201
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 7184-7201
  • 21
    • 77952602864 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 3791-3794
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 3791-3794
  • 43
    • 84873081676 scopus 로고    scopus 로고
    • [9a] However, the yield was lower, and the separation of the stereoisomers only allowed the isolation of the erythro product.
    • Nakatsubo1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.