Convenient synthesis of chiral lignin model compounds via optical resolution: Four stereoisomers of guaiacylglycerol-β-guaiacyl ether and both enantiomers of 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-2-(2-methoxyphenoxy) -propan-1-one (erone)

Tetrahedron Letters

Volumn 53, Issue 7, 2012, Pages 842-845

  Hishiyama, Shojiro ^a,b   Otsuka, Yuichiro ^a   Nakamura, Masaya ^a   Ohara, Seiji ^a   Kajita, Shinya ^b   Masai, Eiji ^c   Katayama, Yoshihiro ^b  

^a FORESTRY AND FOREST PRODUCTS RESEARCH INSTITUTE   (Japan)

^b TOKYO UNIVERSITY OF AGRICULTURE AND TECHNOLOGY   (Japan)

^c NAGAOKA UNIVERSITY OF TECHNOLOGY   (Japan)

Author keywords

Enantiomer; Guaiacylglycerol guaiacyl ether; Lignin; Resolution; Stereochemistry; Synthesis

Indexed keywords

3 HYDROXY 1 (4 HYDROXY 3 METHOXYPHENYL) 2 (2 METHOXYPHENOXY)PROPAN 1 ONE; ALCOHOL; GUAIACYLGLYCEROL 2 GUAIACOL ETHER; LIGNIN; OXIDOREDUCTASE; UNCLASSIFIED DRUG;

ARTICLE; ENANTIOMER; GRAM NEGATIVE BACTERIUM; OPTICAL RESOLUTION; SPHINGOMONAS PAUCIMOBILIS; STEREOCHEMISTRY; STEREOISOMERISM; SYNTHESIS;

NEGIBACTERIA; SPHINGOBIUM; SPHINGOMONAS PAUCIMOBILIS;

EID: 84855825283     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.12.016     Document Type: Article

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