551 related articles for article (PubMed ID: 17048854)
1. Trisubstituted aziridine ring-opening by phenol derivatives: stereo- and regioselective formation of chiral tertiary alkyl-aryl ethers.
Li P; Forbeck EM; Evans CD; Joullié MM
Org Lett; 2006 Oct; 8(22):5105-7. PubMed ID: 17048854
[TBL] [Abstract][Full Text] [Related]
2. A regio- and stereoselective approach to quaternary centers from chiral trisubstituted aziridines.
Forbeck EM; Evans CD; Gilleran JA; Li P; Joullié MM
J Am Chem Soc; 2007 Nov; 129(46):14463-9. PubMed ID: 17973389
[TBL] [Abstract][Full Text] [Related]
3. Ring opening of a resin-bound chiral aziridine with phenol nucleophiles.
Ottesen LK; Jaroszewski JW; Franzyk H
J Org Chem; 2010 Aug; 75(15):4983-91. PubMed ID: 20617832
[TBL] [Abstract][Full Text] [Related]
4. Ring opening of a trisubstituted aziridine with amines: regio- and stereoselective formation of substituted 1,2-diamines.
Kelley BT; Joullié MM
Org Lett; 2010 Oct; 12(19):4244-7. PubMed ID: 20812750
[TBL] [Abstract][Full Text] [Related]
5. A convergent total synthesis of ustiloxin D via an unprecedented copper-catalyzed ethynyl aziridine ring-opening by phenol derivatives.
Li P; Evans CD; Joullié MM
Org Lett; 2005 Nov; 7(23):5325-7. PubMed ID: 16268569
[TBL] [Abstract][Full Text] [Related]
6. Synthesis of (+)-lycoricidine by the application of oxidative and regioselective ring-opening of aziridines.
Yadav JS; Satheesh G; Murthy CV
Org Lett; 2010 Jun; 12(11):2544-7. PubMed ID: 20441205
[TBL] [Abstract][Full Text] [Related]
7. Solvent- and temperature-dependent functionalisation of enantioenriched aziridines.
de Ceglie MC; Musio B; Affortunato F; Moliterni A; Altomare A; Florio S; Luisi R
Chemistry; 2011 Jan; 17(1):286-96. PubMed ID: 21207624
[TBL] [Abstract][Full Text] [Related]
8. Organolithium-induced alkylative ring opening of aziridines: synthesis of unsaturated amino alcohols and ethers.
Hodgson DM; Stefane B; Miles TJ; Witherington J
J Org Chem; 2006 Oct; 71(22):8510-5. PubMed ID: 17064027
[TBL] [Abstract][Full Text] [Related]
9. BF3 x OEt2-mediated highly regioselective S(N)2-type ring-opening of N-activated aziridines and N-activated azetidines by tetraalkylammonium halides.
Ghorai MK; Kumar A; Tiwari DP
J Org Chem; 2010 Jan; 75(1):137-51. PubMed ID: 19968243
[TBL] [Abstract][Full Text] [Related]
10. NaI-catalyzed highly regioselective ring-opening [1 + 2] cycloaddition reaction of cyclopropenes with imines: highly stereoselective synthesis of cis-vinylic aziridines.
Ma S; Zhang J; Lu L; Jin X; Cai Y; Hou H
Chem Commun (Camb); 2005 Feb; (7):909-11. PubMed ID: 15700078
[TBL] [Abstract][Full Text] [Related]
11. Lewis acid catalyzed highly stereoselective domino-ring-opening cyclization of activated aziridines with enolates: synthesis of functionalized chiral γ-lactams.
Ghorai MK; Tiwari DP
J Org Chem; 2010 Sep; 75(18):6173-81. PubMed ID: 20707384
[TBL] [Abstract][Full Text] [Related]
12. Mild metal-free syn-stereoselective ring opening of activated epoxides and aziridines with aryl borates.
Pineschi M; Bertolini F; Haak RM; Crotti P; Macchia F
Chem Commun (Camb); 2005 Mar; (11):1426-8. PubMed ID: 15756325
[TBL] [Abstract][Full Text] [Related]
13. Stereoselective synthesis of trans- and cis-2-aryl-3-(hydroxymethyl)aziridines through transformation of 4-aryl-3-chloro-beta-lactams and study of their ring opening.
D'hooghe M; Mollet K; Dekeukeleire S; De Kimpe N
Org Biomol Chem; 2010 Feb; 8(3):607-15. PubMed ID: 20090977
[TBL] [Abstract][Full Text] [Related]
14. Stereoselective syntheses of 4-oxa diaminopimelic acid and its protected derivatives via aziridine ring opening.
Liu H; Pattabiraman VR; Vederas JC
Org Lett; 2007 Oct; 9(21):4211-4. PubMed ID: 17850092
[TBL] [Abstract][Full Text] [Related]
15. Asymmetric meso-aziridine ring-opening reactions using a chiral zirconium catalyst.
Seki K; Yu R; Yamazaki Y; Yamashita Y; Kobayashi S
Chem Commun (Camb); 2009 Oct; (38):5722-4. PubMed ID: 19774248
[TBL] [Abstract][Full Text] [Related]
16. General, mild, and intermolecular Ullmann-type synthesis of diaryl and alkyl aryl ethers catalyzed by diol-copper(I) complex.
Naidu AB; Jaseer EA; Sekar G
J Org Chem; 2009 May; 74(10):3675-9. PubMed ID: 19361190
[TBL] [Abstract][Full Text] [Related]
17. Asymmetric route to pyridines bearing a highly functionalized 2-alkyl substituent by aziridine ring-opening reactions.
Savoia D; Alvaro G; Di Fabio R; Gualandi A
J Org Chem; 2007 May; 72(10):3859-62. PubMed ID: 17432914
[TBL] [Abstract][Full Text] [Related]
18. Regio- and stereoselective ring opening of enantiomerically enriched 2-aryl oxetanes and 2-aryl azetidines with aryl borates.
Bertolini F; Crotti S; Di Bussolo V; Macchia F; Pineschi M
J Org Chem; 2008 Nov; 73(22):8998-9007. PubMed ID: 18939882
[TBL] [Abstract][Full Text] [Related]
19. Stereoselective synthesis of 4-(N-mesylamino)-2,3-unsaturated- alpha-O-glycosides via a new glycal-derived vinyl alpha-N-(mesyl)-aziridine.
Di Bussolo V; Romano MR; Pineschi M; Crotti P
Org Lett; 2005 Mar; 7(7):1299-302. PubMed ID: 15787491
[TBL] [Abstract][Full Text] [Related]
20. Benzyl protection of phenols under neutral conditions: palladium-catalyzed benzylations of phenols.
Kuwano R; Kusano H
Org Lett; 2008 May; 10(10):1979-82. PubMed ID: 18402462
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
