148 related articles for article (PubMed ID: 11149832)
1. A stereospecific synthesis of (+/-)-5,8-disubstituted indolizidines and (+/-)-1,4-disubstituted quinolizidines found in poison frog skins.
Michel P; Rassat A; Daly JW; Spande TF
J Org Chem; 2000 Dec; 65(26):8908-18. PubMed ID: 11149832
[TBL] [Abstract][Full Text] [Related]
2. A convenient new route to piperidines, pyrrolizidines, indolizidines, and quinolizidines by cyclization of acetylenic sulfones with beta and gamma-chloroamines. Enantioselective total synthesis of indolizidines (-)-167B, (-)-209D, (-)-209B, and (-)-207A.
Back TG; Nakajima K
J Org Chem; 2000 Jul; 65(15):4543-52. PubMed ID: 10959857
[TBL] [Abstract][Full Text] [Related]
3. Alkaloids in Madagascan frogs (Mantella): pumiliotoxins, indolizidines, quinolizidines, and pyrrolizidines.
Garraffo HM; Caceres J; Daly JW; Spande TF; Andriamaharavo NR; Andriantsiferana M
J Nat Prod; 1993 Jul; 56(7):1016-38. PubMed ID: 8377013
[TBL] [Abstract][Full Text] [Related]
4. A short route toward chiral, polyhydroxylated indolizidines and quinolizidines.
Verhelst SH; Paez Martinez B; Timmer MS; Lodder G; van der Marel GA; Overkleeft HS; van Boom JH
J Org Chem; 2003 Dec; 68(25):9598-603. PubMed ID: 14656083
[TBL] [Abstract][Full Text] [Related]
5. A 1,4-disubstituted quinolizidine from a Madagascan mantelline frog (Mantella).
Jain P; Garraffo HM; Yeh HJ; Spande TF; Daly JW; Andriamaharavo NR; Andriantsiferana M
J Nat Prod; 1996 Dec; 59(12):1174-8. PubMed ID: 8988603
[TBL] [Abstract][Full Text] [Related]
6. Synthetic applications of sulfur-substituted indolizidines and quinolizidines.
Chou SS; Chung YC; Chen PA; Chiang SL; Wu CJ
J Org Chem; 2011 Jan; 76(2):692-5. PubMed ID: 21162589
[TBL] [Abstract][Full Text] [Related]
7. A concise and convergent route to 5,8-disubstituted indolizidine and 1,4-disubstituted quinolizidine ring cores by diastereoselective aza-Diels-Alder reaction.
Barluenga J; Mateos C; Aznar F; Valdés C
Org Lett; 2002 May; 4(11):1971-4. PubMed ID: 12027660
[TBL] [Abstract][Full Text] [Related]
8. Alkaloids from bufonid toads (Melanophryniscus): decahydroquinolines, pumiliotoxins and homopumiliotoxins, indolizidines, pyrrolizidines, and quinolizidines.
Garraffo HM; Spande TF; Daly JW; Baldessari A; Gros EG
J Nat Prod; 1993 Mar; 56(3):357-73. PubMed ID: 8482947
[TBL] [Abstract][Full Text] [Related]
9. A one-pot formal [4 + 2] cycloaddition approach to substituted piperidines, indolizidines, and quinolizidines. total synthesis of indolizidine (-)-209I.
Yu S; Zhu W; Ma D
J Org Chem; 2005 Sep; 70(18):7364-70. PubMed ID: 16122260
[TBL] [Abstract][Full Text] [Related]
10. Flexible synthesis of poison-frog alkaloids of the 5,8-disubstituted indolizidine-class. II: Synthesis of (-)-209B, (-)-231C, (-)-233D, (-)-235B", (-)-221I, and an epimer of 193E and pharmacological effects at neuronal nicotinic acetylcholine receptors.
Kobayashi S; Toyooka N; Zhou D; Tsuneki H; Wada T; Sasaoka T; Sakai H; Nemoto H; Garraffo HM; Spande TF; Daly JW
Beilstein J Org Chem; 2007; 3():30. PubMed ID: 21931443
[TBL] [Abstract][Full Text] [Related]
11. Concise enantioselective synthesis of 3,5-dialkyl-substituted indolizidine alkaloids via sequential cross-metathesis-double-reductive cyclization.
Randl S; Blechert S
J Org Chem; 2003 Nov; 68(23):8879-82. PubMed ID: 14604357
[TBL] [Abstract][Full Text] [Related]
12. Indolizidine 239Q and quinolizidine 275I. Major alkaloids in two Argentinian bufonid toads (Melanophryniscus).
Daly JW; Garraffo HM; Spande TF; Yeh HJ; Peltzer PM; Cacivio PM; Baldo JD; Faivovich J
Toxicon; 2008 Dec; 52(8):858-70. PubMed ID: 18848574
[TBL] [Abstract][Full Text] [Related]
13. Alkaloid 223A: the first trisubstituted indolizidine from dendrobatid frogs.
Garraffo HM; Jain P; Spande TF; Daly JW
J Nat Prod; 1997 Jan; 60(1):2-5. PubMed ID: 9014346
[TBL] [Abstract][Full Text] [Related]
14. Ammonia chemical ionization tandem mass spectrometry in structure determination of alkaloids. I. Pyrrolidines, piperidines, decahydroquinolines, pyrrolizidines, indolizidines, quinolizidines and an azabicyclo[5.3.0]decane.
Garraffo HM; Spande TF; Jones TH; Daly JW
Rapid Commun Mass Spectrom; 1999; 13(15):1553-63. PubMed ID: 10421897
[TBL] [Abstract][Full Text] [Related]
15. Alkaloids from a panamanian poison frog, Dendrobates speciosus: identification of pumiliotoxin-A and allopumiliotoxin class alkaloids, 3,5-disubstituted indolizidines, 5-substituted 8-methylindolizidines, and a 2-methyl-6-nonyl-4-hydroxypiperidine.
Edwards MW; Daly JW; Myers CW
J Nat Prod; 1988; 51(6):1188-97. PubMed ID: 3236011
[TBL] [Abstract][Full Text] [Related]
16. Asymmetric synthesis of (-)-1-hydroxyquinolizidinone, a common intermediate for the syntheses of (-)-homopumiliotoxin 223G and (-)-epiquinamide.
Voituriez A; Ferreira F; Pérez-Luna A; Chemla F
Org Lett; 2007 Nov; 9(23):4705-8. PubMed ID: 17929934
[TBL] [Abstract][Full Text] [Related]
17. A flexible approach toward trisubstituted piperidines and indolizidines: synthesis of 6-epi-indolizidine 223A.
Harris JM; Padwa A
J Org Chem; 2003 May; 68(11):4371-81. PubMed ID: 12762739
[TBL] [Abstract][Full Text] [Related]
18. Determining the scope of the organolanthanide-catalyzed, sequential intramolecular amination/cyclization reaction: formation of substituted quinolizidines, indolizidines, and pyrrolizidines.
Molander GA; Pack SK
J Org Chem; 2003 Nov; 68(24):9214-20. PubMed ID: 14629138
[TBL] [Abstract][Full Text] [Related]
19. Kinetic resolution of 2-substituted 2,3-dihydro-4-pyridones by palladium-catalyzed asymmetric allylic alkylation: catalytic asymmetric total synthesis of indolizidine (-)-209I.
Lei BL; Zhang QS; Yu WH; Ding QP; Ding CH; Hou XL
Org Lett; 2014 Apr; 16(7):1944-7. PubMed ID: 24661080
[TBL] [Abstract][Full Text] [Related]
20. Analogues of amphibian alkaloids: total synthesis of (5R,8S,8aS)-(-)-8-methyl-5-pentyloctahydroindolizine (8-epi-indolizidine 209B) and [(1S,4R,9aS)-(-)-4-pentyloctahydro-2H-quinolizin-1-yl]methanol.
Michael JP; Accone C; de Koning CB; van der Westhuyzen CW
Beilstein J Org Chem; 2008 Jan; 4():5. PubMed ID: 18205934
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]