New serinolic amino-s-triazines by chemoselective amination of cyanuric chloride and their (pro)diastereomerism in restricted rotational phenomena

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New serinolic amino-s-triazines by chemoselective amination of cyanuric chloride and their (pro)diastereomerism in restricted rotational phenomena

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wetenschappelijk artikel

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наукова стаття, опублікована в січні 2012

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New serinolic amino-s-triazine ...... estricted rotational phenomena

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New serinolic amino-s-triazine ...... of cyanuric chloride and their

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New serinolic amino-s-triazine ...... estricted rotational phenomena

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New serinolic amino-s-triazine ...... of cyanuric chloride and their

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New serinolic amino-s-triazine ...... estricted rotational phenomena

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New serinolic amino-s-triazine ...... of cyanuric chloride and their

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P1476

New serinolic amino-s-triazine ...... estricted rotational phenomena

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P2093

Agathe Martinez

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Carmen Sacalis

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Dominique Harakat

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Eric Henon

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Flavia Popa

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Mircea Darabantu

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Oana Moldovan

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Pedro Lameiras

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Yvan Ramondenc

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P2860

Synthesis and manipulation of orthogonally protected dendrimers: building blocks for library synthesis.

Triazine dendrimers with orthogonally protected amines on the periphery. Masking amines with Dde and BOC groups provides an alternative to carrying protected alcohols and disulfides through an iterative synthesis.

Electrophoretic Behavior of Anionic Triazine and PAMAM Dendrimers: Methods for Improving Resolution and Assessing Purity Using Capillary Electrophoresis.

Conformational Analysis of Triazine Dendrimers: Using NMR Spectroscopy To Probe the Choreography of a Dendrimer's Dance.

Dendrimers as drug delivery vehicles: non-covalent interactions of bioactive compounds with dendrimers.

Dendrimers Based on [1,3,5]-Triazines.

Orthogonal, convergent syntheses of dendrimers based on melamine with one or two unique surface sites for manipulation.

Steric hindrance to the solvation of melamines and consequences for non-covalent synthesis.

Evaluation of multivalent dendrimers based on melamine: kinetics of thiol-disulfide exchange depends on the structure of the dendrimer.

Toward the next-generation drug delivery vehicle: synthesis of a dendrimer with four orthogonally reactive groups.

P31

scholarly article

P356

10.2478/S11532-012-0015-4

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P433

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P478

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P577

2012-01-01T00:00:00Z

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