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Chemistry - An Asian Journal

Volumn 10, Issue 4, 2015, Pages 869-872

Synthesis of indole terpenoid mimics through a functionality-tolerated Eu(fod)3-catalyzed conjugate addition

(8) Xiong, Xiaochun a,b,c Zhang, Deliang b Li, Jian b Sun, Yu b Zhou, Shupeng b Yang, Ming b Shao, Huawu a Li, Ang b

a CHENGDU INSTITUTE OF BIOLOGY (China)

b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY (China)

c UNIVERSITY OF CHINESE ACADEMY OF SCIENCES (China)

Author keywords

conjugate addition; europium; indoles; natural products; , unsaturated enones

Indexed keywords

ADDITION REACTIONS; CATALYSIS; EUROPIUM; FUNCTIONAL GROUPS; LIPIDS; SYNTHESIS (CHEMICAL);

ACID SENSITIVES; CONJUGATE ADDITION; CONJUGATE ADDITION REACTIONS; INDOLES; NATURAL PRODUCTS; TERPENOIDS;

POLYCYCLIC AROMATIC HYDROCARBONS;

INDOLE DERIVATIVE; ORGANOMETALLIC COMPOUND; TERPENE; TRIS(1,1,1,2,2,3,3-HEPTAFLUORO-7,7-DIMETHYL-4,6- OCTANEDIONATO)EUROPIUM(III);

CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; SYNTHESIS;

CATALYSIS; INDOLES; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; TERPENES;

EID: 84925444061 PISSN: 18614728 EISSN: 1861471X Source Type: Journal
DOI: 10.1002/asia.201403312 Document Type: Article

Times cited : (21)

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