177 related articles for article (PubMed ID: 22118411)
1. Straightforward access to enantioenriched 2-allylpiperidine: application to the synthesis of alkaloids.
Bosque I; González-Gómez JC; Foubelo F; Yus M
J Org Chem; 2012 Jan; 77(1):780-4. PubMed ID: 22118411
[TBL] [Abstract][Full Text] [Related]
2. Preparation of enantiopure substituted piperidines containing 2-alkene or 2-alkyne chains: application to total syntheses of natural quinolizidine-alkaloids.
Cheng G; Wang X; Su D; Liu H; Liu F; Hu Y
J Org Chem; 2010 Mar; 75(6):1911-6. PubMed ID: 20155953
[TBL] [Abstract][Full Text] [Related]
3. Stereoselective synthesis of 2,6-disubstituted piperidines using the iridium-catalyzed allylic cyclization as configurational switch: asymmetric total synthesis of (+)-241 d and related piperidine alkaloids.
Gnamm C; Krauter CM; Brödner K; Helmchen G
Chemistry; 2009; 15(9):2050-4. PubMed ID: 19180605
[TBL] [Abstract][Full Text] [Related]
4. Synthetic approaches to racemic porantheridine and 8-epihalosaline via a nitroso Diels-Alder cycloaddition/ring-rearrangement metathesis sequence.
Sancibrao P; Karila D; Kouklovsky C; Vincent G
J Org Chem; 2010 Jun; 75(12):4333-6. PubMed ID: 20504007
[TBL] [Abstract][Full Text] [Related]
5. Remote stereocenter discrimination in the enzymatic resolution of piperidine-2-ethanol. Short enantioselective synthesis of sedamine and allosedamine.
Angoli M; Barilli A; Lesma G; Passarella D; Riva S; Silvani A; Danieli B
J Org Chem; 2003 Nov; 68(24):9525-7. PubMed ID: 14629188
[TBL] [Abstract][Full Text] [Related]
6. A configurational switch based on iridium-catalyzed allylic cyclization: application in asymmetric total syntheses of prosopis, dendrobate, and spruce alkaloids.
Gnamm C; Brödner K; Krauter CM; Helmchen G
Chemistry; 2009 Oct; 15(40):10514-32. PubMed ID: 19731272
[TBL] [Abstract][Full Text] [Related]
7. Versatile approach to enantiopure 2,6-disubstituted piperidin-3-ol framework: application to the total synthesis of (+)-deoxoprosopinine.
Wang Q; Sasaki NA
J Org Chem; 2004 Jul; 69(14):4767-73. PubMed ID: 15230600
[TBL] [Abstract][Full Text] [Related]
8. Biomimetic organocatalytic asymmetric synthesis of 2-substituted piperidine-type alkaloids and their analogues.
Monaco MR; Renzi P; Scarpino Schietroma DM; Bella M
Org Lett; 2011 Sep; 13(17):4546-9. PubMed ID: 21812495
[TBL] [Abstract][Full Text] [Related]
9. Enantiopure 2,6-disubstituted piperidines bearing one alkene- or alkyne-containing substituent: preparation and application to total syntheses of indolizidine-alkaloids.
Liu H; Su D; Cheng G; Xu J; Wang X; Hu Y
Org Biomol Chem; 2010 Apr; 8(8):1899-904. PubMed ID: 20449496
[TBL] [Abstract][Full Text] [Related]
10. Efficient total synthesis of (+)-dihydropinidine, (-)-epidihydropinidine, and (-)-pinidinone.
Kavala M; Mathia F; Kožíšek J; Szolcsányi P
J Nat Prod; 2011 Apr; 74(4):803-8. PubMed ID: 21410219
[TBL] [Abstract][Full Text] [Related]
11. Synthesis of 2,4,6-trisubstituted chiral piperidines and (-)-dendroprimine by one-pot asymmetric azaelectrocyclization protocol.
Kobayashi T; Hasegawa F; Tanaka K; Katsumura S
Org Lett; 2006 Aug; 8(17):3813-6. PubMed ID: 16898824
[TBL] [Abstract][Full Text] [Related]
12. Stereoselective synthesis of anti-1,3-aminoalcohols via reductive opening of 4-amidotetrahydropyrans derived from the Prins/Ritter sequence.
Yadav JS; Reddy YJ; Reddy PA; Reddy BV
Org Lett; 2013 Feb; 15(3):546-9. PubMed ID: 23339329
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of (-)-deoxoprosophylline, (+)-2-epi-deoxoprosopinine, and (2R,3R)- and (2R,3S)-3-hydroxypipecolic acids from D-glycals.
Kokatla HP; Lahiri R; Kancharla PK; Doddi VR; Vankar YD
J Org Chem; 2010 Jul; 75(13):4608-11. PubMed ID: 20524655
[TBL] [Abstract][Full Text] [Related]
14. Polysubstituted piperidines via iodolactonization: application to the asymmetric synthesis of (+)-pseudodistomin D.
Davies SG; Fletcher AM; Lee JA; Roberts PM; Russell AJ; Taylor RJ; Thomson AD; Thomson JE
Org Lett; 2012 Apr; 14(7):1672-5. PubMed ID: 22416848
[TBL] [Abstract][Full Text] [Related]
15. Synthesis of (R)-dihydropyridones as key intermediates for an efficient access to piperidine alkaloids.
Tzanetou EN; Kasiotis KM; Magiatis P; Haroutounian SA
Molecules; 2007 Apr; 12(4):735-44. PubMed ID: 17851426
[TBL] [Abstract][Full Text] [Related]
16. Total synthesis of dendrobate alkaloid (+)-241D, isosolenopsin and isosolenopsin A: application of a gold-catalyzed cyclization.
Gouault N; Le Roch M; Pinto Gde C; David M
Org Biomol Chem; 2012 Aug; 10(29):5541-6. PubMed ID: 22710861
[TBL] [Abstract][Full Text] [Related]
17. Access to 2,6-disubstituted piperidines: control of the diastereoselectivity, scope, and limitations. Applications to the stereoselective synthesis of (-)-solenopsine A and alkaloid (+)-241D.
Abrunhosa-Thomas I; Plas A; Vogrig A; Kandepedu N; Chalard P; Troin Y
J Org Chem; 2013 Mar; 78(6):2511-26. PubMed ID: 23397886
[TBL] [Abstract][Full Text] [Related]
18. Highly enantioselective synthesis of chiral cyclic amino alcohols and conhydrine by ruthenium-catalyzed asymmetric hydrogenation.
Liu S; Xie JH; Li W; Kong WL; Wang LX; Zhou QL
Org Lett; 2009 Nov; 11(21):4994-7. PubMed ID: 19788265
[TBL] [Abstract][Full Text] [Related]
19. Stereocontrolled synthesis of vicinal diamines by organocatalytic asymmetric Mannich reaction of N-protected aminoacetaldehydes: formal synthesis of (-)-agelastatin A.
Kano T; Sakamoto R; Akakura M; Maruoka K
J Am Chem Soc; 2012 May; 134(17):7516-20. PubMed ID: 22486203
[TBL] [Abstract][Full Text] [Related]
20. Short asymmetric synthesis of phenanthroindolizidines through chiral homoallylic sulfinamines.
Anton-Torrecillas C; Gonzalez-Gomez JC
Org Biomol Chem; 2014 Sep; 12(36):7018-25. PubMed ID: 25070561
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
