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Items: 1 to 20 of 128

2.

The synthesis and characterization of all diastereomers of a linear symmetrically fused Tris-Tröger's base analogue: new chiral cleft compounds.

Artacho J, Nilsson P, Bergquist KE, Wendt OF, Wärnmark K.

Chemistry. 2006 Mar 20;12(10):2692-701.

PMID:
16429475
4.

Tröger's base. An alternate synthesis and a structural analog with thromboxane A2 synthetase inhibitory activity.

Johnson RA, Gorman RR, Wnuk RJ, Crittenden NJ, Aiken JW.

J Med Chem. 1993 Oct 15;36(21):3202-6.

PMID:
8230108
5.

5,12-Dimethyl-3,10-diphenyl-1,3,4,8,10,11-hexaazatetracyclo[6.6.1.0(2,6).0(9,13)]pentadeca-2(6),4,9,(13),11-tetraene,a new Tröger's base analogue.

Moreno-Fuquen R, Abonia R, Valderrama-Naranjo J, Albornoz A, Mariezcurrena RA.

Acta Crystallogr C. 2001 Mar;57(Pt 3):281-3.

PMID:
11250578
6.

calix-Tris-Tröger's bases--a new cavitand family.

Valík M, Cejka J, Havlík M, Král V, Dolenský B.

Chem Commun (Camb). 2007 Oct 7;(37):3835-7.

PMID:
18217663
7.

Probing the stereointegrity of Tröger's base--a dynamic electrokinetic chromatographic study.

Trapp O, Trapp G, Kong J, Hahn U, Vögtle F, Schurig V.

Chemistry. 2002 Aug 16;8(16):3629-34.

PMID:
12203289
8.

Discovery of Tröger's base analogues as selective inhibitors against human breast cancer cell line: design, synthesis and cytotoxic evaluation.

Manda BR, Alla M, Ganji RJ, Addlagatta A.

Eur J Med Chem. 2014 Oct 30;86:39-47. doi: 10.1016/j.ejmech.2014.08.044.

PMID:
25140752
9.

Stepwise Replication of a Tröger's Base Analogue.

Bag BG, von Kiedrowski G.

Angew Chem Int Ed Engl. 1999 Dec 16;38(24):3713-3714.

PMID:
10649334
10.

Tröger's base twisted amides: endo functionalization and synthesis of an inverted crown ether.

Artacho J, Ascic E, Rantanen T, Wallentin CJ, Dawaigher S, Bergquist KE, Harmata M, Snieckus V, Wärnmark K.

Org Lett. 2012 Sep 21;14(18):4706-9.

PMID:
22958089
11.

(1)H and (13)C NMR studies of asymmetrically substituted bis- and tris-Tröger's bases.

Elguero J, Fruchier A, Mas T, Pardo C.

Magn Reson Chem. 2005 Aug;43(8):665-9.

PMID:
15986498
12.

Synthesis of enantiomerically pure Tröger's base derivatives via chiral disulfoxides.

Ondrisek P, Schwenk R, Cvengroš J.

Chem Commun (Camb). 2014 Aug 21;50(65):9168-71. doi: 10.1039/c4cc03963g.

PMID:
24993027
13.

Adsorption behavior of the (+/-)-Tröger's base enantiomers in the phase system of a silica-based packing coated with amylose tri(3,5-dimethyl carbamate) and 2-propanol and molecular modeling interpretation.

Mihlbachler K, De Jesús MA, Kaczmarski K, Sepaniak MJ, Seidel-Morgenstern A, Guiochon G.

J Chromatogr A. 2006 Apr 28;1113(1-2):148-61.

PMID:
16516901
14.

Symmetrical and nonsymmetrical chromophores with Tröger's base skeleton: chiroptical, linear, and quadratic nonlinear optical properties--a joint theoretical and experimental study.

Sergeyev S, Didier D, Boitsov V, Teshome A, Asselberghs I, Clays K, Vande Velde CM, Plaquet A, Champagne B.

Chemistry. 2010 Jul 19;16(27):8181-90. doi: 10.1002/chem.201000216.

PMID:
20533454
15.

Synthesis, resolution, and absolute configuration of difunctionalized Tröger's base derivatives.

Kiehne U, Bruhn T, Schnakenburg G, Fröhlich R, Bringmann G, Lützen A.

Chemistry. 2008;14(14):4246-55. doi: 10.1002/chem.200701960.

PMID:
18351700
16.

Diastereoselective self-assembly of double-stranded helicates from Tröger's base derivatives.

Kiehne U, Weilandt T, Lützen A.

Org Lett. 2007 Mar 29;9(7):1283-6.

PMID:
17346054
17.

Oligo Tröger's bases--new molecular scaffolds.

Dolenský B, Havlík M, Král V.

Chem Soc Rev. 2012 May 21;41(10):3839-58. doi: 10.1039/c2cs15307f.

PMID:
22441244
18.

A Protocol for the exo-Mono and exo,exo-Bis Functionalization of the Diazocine Ring of Tröger's Base.

Dawaigher S, Månsson K, Ascic E, Artacho J, Mårtensson R, Loganathan N, Wendt OF, Harmata M, Snieckus V, Wärnmark K.

J Org Chem. 2015 Dec 18;80(24):12006-14. doi: 10.1021/acs.joc.5b01921.

PMID:
26597045
19.

Resolution and Determination of the Absolute Configuration of a Twisted Bis-Lactam Analogue of Tröger's Base: A Comparative Spectroscopic and Computational Study.

Rúnarsson ÖV, Benkhäuser C, Christensen NJ, Ruiz JA, Ascic E, Harmata M, Snieckus V, Rissanen K, Fristrup P, Lützen A, Wärnmark K.

J Org Chem. 2015 Aug 21;80(16):8142-9. doi: 10.1021/acs.joc.5b01236.

PMID:
26244379
20.

Application of crystallization-induced asymmetric transformation to a general, scalable method for the resolution of 2,8-disubstituted Tröger's base derivatives.

Jameson DL, Field T, Schmidt MR, DeStefano AK, Stiteler CJ, Venditto VJ, Krovic B, Hoffman CM, Ondisco MT, Belowich ME.

J Org Chem. 2013 Nov 15;78(22):11590-6. doi: 10.1021/jo401873x.

PMID:
24116701
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