149 related articles for article (PubMed ID: 26824669)
1. Stereoselective Synthesis of Isochromanones by an Asymmetric Ortho-Lithiation Strategy: Synthetic Access to the Isochromanone Core of the Ajudazols.
Essig S; Menche D
J Org Chem; 2016 Mar; 81(5):1943-66. PubMed ID: 26824669
[TBL] [Abstract][Full Text] [Related]
2. Stereoselective synthesis of novel highly substituted isochromanone and isoquinolinone-containing exocyclic tetrasubstituted alkenes.
Arthuis M; Pontikis R; Florent JC
J Org Chem; 2009 Mar; 74(5):2234-7. PubMed ID: 19199667
[TBL] [Abstract][Full Text] [Related]
3. Full stereochemical determination of ajudazols A and B by bioinformatics gene cluster analysis and total synthesis of ajudazol B by an asymmetric ortholithiation strategy.
Essig S; Bretzke S; Müller R; Menche D
J Am Chem Soc; 2012 Nov; 134(47):19362-5. PubMed ID: 23127125
[TBL] [Abstract][Full Text] [Related]
4. Direct Enantioselective and Regioselective Alkylation of β,γ-Unsaturated Carboxylic Acids with Chiral Lithium Amides as Traceless Auxiliaries.
Yu K; Miao B; Wang W; Zakarian A
Org Lett; 2019 Mar; 21(6):1930-1934. PubMed ID: 30835486
[TBL] [Abstract][Full Text] [Related]
5. Asymmetric construction of quaternary carbon centers by sequential conjugate addition of lithium amide and in situ alkylation: utility in the synthesis of (-)-aspidospermidine.
Suzuki M; Kawamoto Y; Sakai T; Yamamoto Y; Tomioka K
Org Lett; 2009 Feb; 11(3):653-5. PubMed ID: 19115978
[TBL] [Abstract][Full Text] [Related]
6. Synthesis and C-alkylation of hindered aldehyde enamines.
Hodgson DM; Bray CD; Kindon ND; Reynolds NJ; Coote SJ; Um JM; Houk KN
J Org Chem; 2009 Feb; 74(3):1019-28. PubMed ID: 19105636
[TBL] [Abstract][Full Text] [Related]
7. Highly enantioselective direct alkylation of arylacetic acids with chiral lithium amides as traceless auxiliaries.
Stivala CE; Zakarian A
J Am Chem Soc; 2011 Aug; 133(31):11936-9. PubMed ID: 21744818
[TBL] [Abstract][Full Text] [Related]
8. Predictive Bioinformatic Assignment of Methyl-Bearing Stereocenters, Total Synthesis, and an Additional Molecular Target of Ajudazol B.
Essig S; Schmalzbauer B; Bretzke S; Scherer O; Koeberle A; Werz O; Müller R; Menche D
J Org Chem; 2016 Feb; 81(4):1333-57. PubMed ID: 26796481
[TBL] [Abstract][Full Text] [Related]
9. The diarylprolinol silyl ether system: a general organocatalyst.
Jensen KL; Dickmeiss G; Jiang H; Albrecht L; Jørgensen KA
Acc Chem Res; 2012 Feb; 45(2):248-64. PubMed ID: 21848275
[TBL] [Abstract][Full Text] [Related]
10. Asymmetric synthesis of syn-alpha-substituted beta-amino ketones by using sulfinimines and prochiral Weinreb amide enolates.
Davis FA; Song M
Org Lett; 2007 Jun; 9(12):2413-6. PubMed ID: 17497798
[TBL] [Abstract][Full Text] [Related]
11. Synthesis of Enantiopure Piperazines via Asymmetric Lithiation-Trapping of N-Boc Piperazines: Unexpected Role of the Electrophile and Distal N-Substituent.
Firth JD; O'Brien P; Ferris L
J Am Chem Soc; 2016 Jan; 138(2):651-9. PubMed ID: 26683825
[TBL] [Abstract][Full Text] [Related]
12. A direct and general method for the reductive alkylation of tertiary lactams/amides: application to the step economical synthesis of alkaloid (-)-morusimic acid D.
Xiao KJ; Wang Y; Huang YH; Wang XG; Huang PQ
J Org Chem; 2013 Sep; 78(17):8305-11. PubMed ID: 23909394
[TBL] [Abstract][Full Text] [Related]
13. Use of lithiated chiral o-sulfinylbenzyl carbanions for the one-pot building of linear fragments containing up to four connected stereocenters.
García Ruano JL; Torrente E; Martín-Castro AM
J Org Chem; 2013 Jan; 78(2):647-57. PubMed ID: 23256861
[TBL] [Abstract][Full Text] [Related]
14. Reactions of 3-isochromanone with aromatic aldehydes--microwave assisted condensations performed on solid basic inorganic supports.
Vass A; Földesi A; Lóránd T
J Biochem Biophys Methods; 2006 Nov; 69(1-2):179-87. PubMed ID: 16678272
[TBL] [Abstract][Full Text] [Related]
15. Synthesis of 2-alkyl-substituted chromone derivatives using microwave irradiation.
Fridén-Saxin M; Pemberton N; Andersson Kda S; Dyrager C; Friberg A; Grøtli M; Luthman K
J Org Chem; 2009 Apr; 74(7):2755-9. PubMed ID: 19323574
[TBL] [Abstract][Full Text] [Related]
16. Highly anti-selective catalytic aldol reactions of amides with aldehydes.
Saito S; Kobayashi S
J Am Chem Soc; 2006 Jul; 128(27):8704-5. PubMed ID: 16819844
[TBL] [Abstract][Full Text] [Related]
17. Asymmetric synthesis of 3,4-anti- and 3,4-syn-substituted aminopyrrolidines via lithium amide conjugate addition.
Davies SG; Garner AC; Goddard EC; Kruchinin D; Roberts PM; Smith AD; Rodriguez-Solla H; Thomson JE; Toms SM
Org Biomol Chem; 2007 Jun; 5(12):1961-9. PubMed ID: 17551646
[TBL] [Abstract][Full Text] [Related]
18. Rearrangement of spirocyclic oxindoles with lithium amide bases.
Rousseau G; Robert F; Schenk K; Landais Y
Org Lett; 2008 Oct; 10(20):4441-4. PubMed ID: 18783229
[TBL] [Abstract][Full Text] [Related]
19. A general approach to high-yielding asymmetric synthesis of chiral 3-alkyl-4-nitromethylchromans via cascade Barbas-Michael and acetalization reactions.
Ramachary DB; Prasad MS; Madhavachary R
Org Biomol Chem; 2011 Apr; 9(8):2715-21. PubMed ID: 21369625
[TBL] [Abstract][Full Text] [Related]
20. Lithiation of N-alkyl-(o-tolyl)aziridine: stereoselective synthesis of isochromans.
Dammacco M; Degennaro L; Florio S; Luisi R; Musio B; Altomare A
J Org Chem; 2009 Aug; 74(16):6319-22. PubMed ID: 19610596
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]