Stereoselective formal synthesis of (-)-centrolobine

Tetrahedron

Volumn 63, Issue 5, 2007, Pages 1089-1092

  Prasad, Kavirayani R ^a   Anbarasan, Pazhamalai ^a  

^a INDIAN INSTITUTE OF SCIENCE   (India)

Author keywords

( ) Centrolobine; FeCl3; Stereoselective reduction; Tartaric acid

Indexed keywords

CENTROLOBINE; FERRIC CHLORIDE; NATURAL PRODUCT; TARTARIC ACID; TETRAHYDROPYRAN DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLIZATION; DEPROTECTION REACTION; DIASTEREOISOMER; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTUM YIELD; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 33845681174     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.11.062     Document Type: Article

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32. Formation of the tetrahydropyran 3b in 17% yield was also observed, which on further reaction with aq HCl furnished 3.{A figure is presented}
33. 3)), the spectral data of which is consistent with that reported in literature.