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kw.\*:("PUMILIOTOXINE A")

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Enantioselective total synthesis of (+)-pumiliotoxin AOVERMAN, L. E; NAN-HORNG LIN.Journal of organic chemistry. 1985, Vol 50, Num 19, pp 3669-3670, issn 0022-3263Article

A NEW CLASS OF INDOLIZIDINE ALKALOIDS FROM THE POISON FROG, DENDROBATES TRICOLOR. X-RAY ANALYSIS OF 8-HYDROXY-8-METHYL-6-(2'-METHYLHEXYLIDENE)-1-AZABICYCLO (4.3.0) NONANEDALY JW; TOKUYAMA T; FUJIWARA T et al.1980; J. AMER. CHEM. SOC.; USA; DA. 1980; VOL. 102; NO 2; PP. 830-836; BIBL. 18 REF.Article

CARBONYL PARTICIPATION IN THE REACTION OF N-ACYL-2-ISOPROPENYLPYRROLIDINES WITH HALOGEN ELECTROPHILES. STEREOCONTROLLED PREPARATION OF ENANTIOMERICALLY PURE SYNTHONS FOR THE SYNTHESIS OF PUMILIOTOXIN A ALKALOIDSOVERMAN LE; MCCREADY RJ.1982; TETRAHEDRON LETT.; ISSN 0040-4039; GBR; DA. 1982; VOL. 23; NO 47; PP. 4887-4890; BIBL. 18 REF.Article

Alkaloids in Madagascan frogs (Mantella) : pumiliotoxins, indolizidines, quinolizidines, and pyrrolizidinesGARRAFFO, H. M; CACERES, J; DALY, J. W et al.Journal of natural products (Print). 1993, Vol 56, Num 7, pp 1016-1038, issn 0163-3864Article

Pumiliotoxin alkaloids: relationship of cardiotonic activity to sodium channel activity and phosphatidylinositol turnoverDALY, J. W; MCNEAL, E; GUSOVSKY, F et al.Journal of medicinal chemistry (Print). 1988, Vol 31, Num 2, pp 477-480, issn 0022-2623Article

The synthesis of indolizidines by intramolecular ene cyclizations. Preparation of (E)-alkylidene analogs of pumiliotoxin AOVERMAN, L. E; LESUISSE, D.Tetrahedron letters. 1985, Vol 26, Num 35, pp 4167-4170, issn 0040-4039Article

Enantioselective total synthesis of the pumiliotoxin A alkaloids via reductive iminium ion-alkyne cyclizations. Total synthesis of (+)-pumiliotoxin AOVERMAN, L. E; SHARP, M. J.Tetrahedron letters. 1988, Vol 29, Num 8, pp 901-904, issn 0040-4039Article

Convergent approach to pumiliotoxin alkaloids. Asymmetric total synthesis of (+)-pumiliotoxins A, B, and 225FAOYAGI, Sakae; HIRASHIMA, Shintaro; SAITO, Kosuke et al.Journal of organic chemistry. 2002, Vol 67, Num 16, pp 5517-5526, issn 0022-3263, 10 p.Article

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