Suzuki-Miyaura and stille reactions as key steps in the synthesis of diversely functionalized Amaryllidaceae alkaloid analogs bearing a 5,6,7,8-tetrahydrobenzo[c,e]azocine skeleton

Combinatorial Chemistry and High Throughput Screening

Volumn 10, Issue 9, 2007, Pages 790-801

  Appukkuttan, Prasad ^a,b   Dehaen, Wim ^a   Van Der Eycken, Erik ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b UPPSALA UNIVERSITY   (Sweden)

Author keywords

Biaryl; Cross coupling; Microwave; Natural products; Stille; Suzuki Miyaura

Indexed keywords

5,6,7,8 TETRAHYDROBENZO [C,E] AZOCINE; AMARYLLIDACEAE ALKALOID; AZOCINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; MICROWAVE IRRADIATION; PRIORITY JOURNAL; STILLE REACTION; SYNTHESIS;

AMARYLLIDACEAE ALKALOIDS; AZOCINES; BIOLOGICAL PRODUCTS; CATALYSIS; COMBINATORIAL CHEMISTRY TECHNIQUES; GALANTAMINE; METALS; MICROWAVES; MODELS, CHEMICAL;

AMARYLLIDACEAE;

EID: 37049029035     PISSN: 13862073     EISSN: None     Source Type: Journal    
DOI: 10.2174/138620707783018513     Document Type: Article

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