Literature DB >> 18517213

Synthesis of (+)-uniflorine a: a structural reassignment and a configurational assignment.

Thunwadee Ritthiwigrom1, Stephen G Pyne.   

Abstract

The total synthesis of (+)-uniflorine A has allowed for the structural reassignment and the configurational assignment of the alkaloid (-)-uniflorine A from a 1,2,6,7,8-pentahydroxyindolizidine structure to (-)-(1 R,2 R,3 R,6 R,7 S,7a R)-1,2,6,7-tetrahydroxy-3-hydroxymethylpyrrolizidine (6- epi-casuarine).

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Year:  2008        PMID: 18517213     DOI: 10.1021/ol8009144

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Catalytic diastereoselective petasis reactions.

Authors:  Giovanni Muncipinto; Philip N Moquist; Stuart L Schreiber; Scott E Schaus
Journal:  Angew Chem Int Ed Engl       Date:  2011-07-12       Impact factor: 15.336

2.  Glycerol as an efficient medium for the petasis borono-mannich reaction.

Authors:  Tomi Rosholm; Pedro M P Gois; Robert Franzen; Nuno R Candeias
Journal:  ChemistryOpen       Date:  2014-10-18       Impact factor: 2.911

3.  Reactivity and Synthetic Applications of Multicomponent Petasis Reactions.

Authors:  Peng Wu; Michael Givskov; Thomas E Nielsen
Journal:  Chem Rev       Date:  2019-08-27       Impact factor: 60.622

  3 in total

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