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Enantioselective Synthesis of Key Intermediates in a Novel Approach towards the Iboga ‐Alkaloid Family
Author(s) -
Höck Stefan,
Borschberg HansJürg
Publication year - 2003
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.200390125
Subject(s) - chemistry , cycloaddition , enantioselective synthesis , absolute configuration , diastereomer , stereochemistry , total synthesis , yield (engineering) , intramolecular force , ketone , organic chemistry , materials science , metallurgy , catalysis
Significant improvements in the realm of a recently disclosed, novel synthetic concept towards the Iboga alkaloid family are presented. The key step for the construction of the bicyclic aliphatic core consists of an intramolecular nitroneolefin 1,3‐dipolar cycloaddition reaction of a 1 : 1 mixture 15 / 16 yielding the two diastereoisomeric tricyclic isoxazolidine derivatives 17 and 18 . The required nitrones were prepared from the readily available ( S )‐hydroxylactone 6 in twelve steps with an overall yield of 15% (average: 83.5% per step). The relative configuration of the minor isomer was deduced unambiguously by single‐crystal X‐ray analysis of the derived tricyclic carbamate 21 . As four out of five asymmetric centers in the pair 17 / 18 have opposite configuration, destruction of the one possessing the same absolute configuration transforms the original set of diastereoisomers into a pair of enantiomers. We verified this contention by oxidizing the two alcohols 20 and 22 to yield the two antipodal forms of ketone 23 . The absence of significant amounts of by‐product and the high reproducibility of the crucial cycloaddition reaction represent marked improvements over our earlier attempts. In addition, the new route, which starts from L ‐glutamate, should provide access to both naturally occurring antipodal series of the targeted alkaloid class.