Naphthol radical couplings determine structural features and enantiomeric excess of dalesconols in Daldinia eschscholzii

Nature Communications

Volumn 3, Issue , 2012, Pages

  Fang, Wei ^a   Ji, Shen ^b   Jiang, Nan ^a,c   Wang, Wei ^a   Zhao, Guo Yan ^a   Zhang, Su ^b   Ge, Hui Ming ^a   Xu, Qiang ^a   Zhang, Ai Hua ^a   Zhang, Ying Lao ^a   Song, Yong Chun ^a   Zhang, Jie ^a   Tan, Ren Xiang ^a  

^a NANJING UNIVERSITY   (China)

^b Shanghai Institute of Food and Drug Controls   (China)

^c NANJING MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

1 NAPHTHOL DERIVATIVE; DALESCONOL; DALESCONOL A; DALESCONOL B; DALESCONOL C; DIMER; IMMUNOSUPPRESSIVE AGENT; LACCASE; POLYKETIDE; RADICAL; UNCLASSIFIED DRUG;

ARTICLE; BIOSYNTHESIS; CHEMICAL STRUCTURE; CONFORMATION; CONTROLLED STUDY; DALDINIA ESCHSCHOLZII; ENANTIOMER; FUNGUS; NONHUMAN; OXIDATIVE COUPLING; STEREOCHEMISTRY;

DIBENZOCYCLOHEPTENES; FREE RADICALS; NAPHTHOLS; POLYCYCLIC HYDROCARBONS, AROMATIC; STEREOISOMERISM; XYLARIALES;

DALDINIA ESCHSCHOLZII; FUNGI; MANTIS;

EID: 84866987140     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms2031     Document Type: Article

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