301 related articles for article (PubMed ID: 21077094)
1. Regioselective ring-opening of amino acid-derived chiral aziridines: an easy access to cis-2,5-disubstituted chiral piperazines.
Samanta K; Panda G
Chem Asian J; 2011 Jan; 6(1):189-97. PubMed ID: 21077094
[TBL] [Abstract][Full Text] [Related]
2. Selectively N-protected enantiopure 2,5-disubstituted piperazines: avoiding the pitfalls in solid-phase Fukuyama-Mitsunobu cyclizations.
Ottesen LK; Olsen CA; Witt M; Jaroszewski JW; Franzyk H
Chemistry; 2009; 15(12):2966-78. PubMed ID: 19191236
[TBL] [Abstract][Full Text] [Related]
3. Expedite protocol for construction of chiral regioselectively N-protected monosubstituted piperazine, 1,4-diazepane, and 1,4-diazocane building blocks.
Crestey F; Witt M; Jaroszewski JW; Franzyk H
J Org Chem; 2009 Aug; 74(15):5652-5. PubMed ID: 19518106
[TBL] [Abstract][Full Text] [Related]
4. One pot synthesis of amino acid derived chiral disubstituted morpholines and 1,4-oxazepanes via tandem aziridine/epoxide ring opening sequences.
Samanta K; Panda G
Org Biomol Chem; 2011 Nov; 9(21):7365-71. PubMed ID: 21863154
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. One-pot preparation of piperazines by regioselective ring-opening of non-activated arylaziridines.
Trinchera P; Musio B; Degennaro L; Moliterni A; Falcicchio A; Luisi R
Org Biomol Chem; 2012 Mar; 10(10):1962-5. PubMed ID: 22286638
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Synthetic route to chiral tetrahydroquinoxalines via ring-opening of activated aziridines.
Ghorai MK; Sahoo AK; Kumar S
Org Lett; 2011 Nov; 13(22):5972-5. PubMed ID: 22004011
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. Alumina-supported Cu(II), a versatile and recyclable catalyst for regioselective ring opening of aziridines and epoxides and subsequent cyclization to functionalized 1,4-benzoxazines and 1,4-benzodioxanes.
Bhadra S; Adak L; Samanta S; Maidul Islam AK; Mukherjee M; Ranu BC
J Org Chem; 2010 Dec; 75(24):8533-41. PubMed ID: 21070034
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Nucleophilic ring-opening of epoxide and aziridine acetates for the stereodivergent synthesis of β-hydroxy and β-amino γ-lactams.
Bisol TB; Bortoluzzi AJ; Sá MM
J Org Chem; 2011 Feb; 76(3):948-62. PubMed ID: 21194209
[TBL] [Abstract][Full Text] [Related]
15. Regioselective and Stereodivergent Synthesis of Enantiomerically Pure
Wosińska-Hrydczuk M; Boratyński PJ; Skarżewski J
Molecules; 2020 Feb; 25(3):. PubMed ID: 32046110
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Synthesis of gem-disubstituted taurines by the regioselective ring-opening of 2,2-disubstituted aziridines with sodium bisulfite and sulfite.
Chen N; Zhu M; Zhang W; Du DM; Xu J
Amino Acids; 2009 Jul; 37(2):309-13. PubMed ID: 18683018
[TBL] [Abstract][Full Text] [Related]
18. Ring opening/C-N cyclization of activated aziridines with carbon nucleophiles: highly diastereo- and enantioselective synthesis of tetrahydroquinolines.
Ghorai MK; Nanaji Y; Yadav AK
Org Lett; 2011 Aug; 13(16):4256-9. PubMed ID: 21766866
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Asymmetric aziridination of cyclic enones using chiral diamine catalysts and its application to the total synthesis of (-)-agelastatin A.
Menjo Y; Hamajima A; Sasaki N; Hamada Y
Org Lett; 2011 Nov; 13(21):5744-7. PubMed ID: 21966984
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
