New routes to clavine-type ergot alkaloids. Part 2: Synthesis of the last, so far not yet synthesized member of the clavine alkaloid family, (±)-cycloclavine

Tetrahedron

Volumn 64, Issue 13, 2008, Pages 2924-2929

  Incze, Mária ^a   Dörnyei, Gábor ^a   Moldvai, István ^a   Temesvári Major, Eszter ^a   Egyed, Orsolya ^a   Szántay, Csaba ^a  

^a CHEMICAL RESEARCH CENTER   (Hungary)

Author keywords

( ) Cycloclavine; Clavine alkaloids; Cyclopropanation with diazomethane; Modified intramolecular Reformatsky type cyclization; Total synthesis from 4 bromo Uhle's ketone

Indexed keywords

ALKALOID DERIVATIVE; CYCLOCLAVINE ERGOT ALKALOID DERIVATIVE; ERGOT ALKALOID; ESTER DERIVATIVE; METHYL GROUP; UNCLASSIFIED DRUG;

ALDOL REACTION; ALKYLATION; ARTICLE; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; CYCLOPROPANATION; INFRARED SPECTROSCOPY; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; SYNTHESIS;

EID: 39149111561     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.01.101     Document Type: Article

References (16)

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