Isolation and biomimetic synthesis of (±)-calliviminones A and B, two novel Diels-Alder adducts, from Callistemon viminalis

Tetrahedron Letters

Volumn 56, Issue 1, 2015, Pages 229-232

  Wu, Lin ^a   Luo, Jun ^a   Zhang, Yalong ^a   Zhu, Mengdi ^a   Wang, Xiaobing ^a   Luo, Jianguang ^a   Yang, Minghua ^a   Yu, Boyang ^a   Yao, Hequan ^a   Dai, Yue ^a   Guo, Qinglong ^a   Chen, Yijun ^a   Sun, Hongbin ^a   Kong, Lingyi ^a  

^a CHINA PHARMACEUTICAL UNIVERSITY   (China)

Author keywords

Biomimetic synthesis; Diels Alder reaction; Spiro compounds; Triketones

Indexed keywords

ANTIINFLAMMATORY AGENT; CALLIVIMINONE A; CALLIVIMINONE B; MYRCENE; PHLOROGLUCINOL; PLANT MEDICINAL PRODUCT; UNCLASSIFIED DRUG;

ARTICLE; BIOSYNTHESIS; CALLISTEMON VIMINALIS; CARBON NUCLEAR MAGNETIC RESONANCE; DIELS ALDER REACTION; DRUG ISOLATION; DRUG SYNTHESIS; ENANTIOMER; HETERONUCLEAR MULTIPLE BOND CORRELATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MYRTACEAE; PROTON NUCLEAR MAGNETIC RESONANCE; RACEMIC MIXTURE;

ALNUS; CALLISTEMON VIMINALIS;

EID: 84918582442     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2014.11.075     Document Type: Article

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