Highly diastereoselective approach to novel phenylindolizidinols via benzothieno analogues of tylophorine based on reductive desulfurization of benzo[b]thiophene

Tetrahedron Asymmetry

Volumn 20, Issue 5, 2009, Pages 626-634

  Šafář, Peter ^a   Žúžiová, Jozefína ^a   Marchalín, Štefan ^a   Tóthová, Eva ^a   Prónayová, Nadežda ^a   Švorc, Ľubomír ^a   Vrábel, Viktor ^a   Daïch, Adam ^b  

^a SLOVAK UNIVERSITY OF TECHNOLOGY   (Slovakia)

^b UNIVERSITÉ DU HAVRE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BENZO[B]THIOPHENE 2 CARBOXALDEHYDE; BENZOTHIOPHENE; CASTANOSPERMINE; GEPHYROTOXIN 223AB; GLUTAMIC ACID; INDOLIZINE DERIVATIVE; LACTAM; MYMICARIN 237A; NATURAL PRODUCT; SWAINSONINE; TYLOPHORINE; UNCLASSIFIED DRUG;

ARTICLE; DESULFURIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROGENOLYSIS; MITSUNOBU REACTION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; REDUCTION; REPRODUCIBILITY; STEREOCHEMISTRY;

EID: 65349096755     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.02.042     Document Type: Article

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