SCOPUS 정보 검색 플랫폼

Volumn 12, Issue 18, 2014, Pages 2859-2863

Complexity generation by chemical synthesis: A five-step synthesis of (-)-chaetominine from l-tryptophan and its biosynthetic implications

(4) Xu, Chu Pei a Luo, Shi Peng a Wang, Ai E a Huang, Pei Qiang a,b

a XIAMEN UNIVERSITY (China)

b LANZHOU UNIVERSITY (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS;

BIOSYNTHETIC PATHWAY; CHEMISTRY PRINCIPLES; EPIMERIZATION; L-TRYPTOPHAN; MOLECULAR COMPLEXITY; REGIO-SELECTIVE; RING OPENING REACTION;

BIOSYNTHESIS;

CHAETOMININE; CYCLOPEPTIDE; INDOLE ALKALOID; KAPAKAHINE B; KAPAKAHINE F; TRYPTOPHAN;

BIOSYNTHESIS; CHEMISTRY; ORGANIC CHEMISTRY; PROCEDURES; SYNTHESIS;

BIOSYNTHETIC PATHWAYS; CHEMISTRY, ORGANIC; INDOLE ALKALOIDS; PEPTIDES, CYCLIC; TRYPTOPHAN;

EID: 84898029092 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c4ob00314d Document Type: Article

Times cited : (24)

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