SCOPUS 정보 검색 플랫폼

Volumn 14, Issue 26, 2016, Pages 6225-6230

Asymmetric synthesis and absolute stereochemistry of a labdane-type diterpenoid isolated from the rhizomes of: Isodan yuennanensis

(4) Deng, Heping a Cao, Wei a Zhang, Zhijiang a Liu, Bo a,b

a Sichuan University (China)

b CHINA PHARMACEUTICAL UNIVERSITY (China)

Author keywords

[No Author keywords available]

Indexed keywords

ESTERS; STEREOCHEMISTRY; STEREOSELECTIVITY;

ABSOLUTE STEREOCHEMISTRY; ASYMMETRIC SYNTHESIS; DITERPENOID; ESTER REACTIONS; METHYL GROUP; SYNTHESIS FEATURES;

LIPIDS;

DITERPENE; ISODAN; LABDANE; METHACRYLIC ACID DERIVATIVE; NITRIC ACID DERIVATIVE; SODIUM FLUORIDE;

CHEMISTRY; CONFORMATION; ISOLATION AND PURIFICATION; RHIZOME; STEREOISOMERISM; SYNTHESIS;

DITERPENES; METHACRYLATES; MOLECULAR CONFORMATION; NITRATES; RHIZOME; SODIUM FLUORIDE; STEREOISOMERISM;

EID: 84976875346 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c6ob00750c Document Type: Article

Times cited : (11)

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