Synthesis of cyclic bis- and trismelamine derivatives and their complexation properties with barbiturates-Reference-Cited by-同舟云学术

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Synthesis of cyclic bis- and trismelamine derivatives and their complexation properties with barbiturates

Published:2007 Issue:6 Volume:5 Page:907
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Kondo Shin-ichi,Hayashi Tomohiro,Sakuno Yuichi,Takezawa Yoko,Yokoyama Takashi,Unno Masafumi,Yano Yumihiko

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2007/OB/B615537E

Reference52 articles.

1. Synthetic Studies on Molecular Recognition

2. Molecular recognition of biologically interesting substrates: synthesis of an artificial receptor for barbiturates employing six hydrogen bonds

3. Hydrogen-bonding self-assembly of multichromophore structures

4. Molecular recognition and catalysis; acceleration of acyl transfer reactions by a hydrogen-bonding receptor

5. Hydrogen bonding and molecular recognition: synthetic, complexation, and structural studies on barbiturate binding to an artificial receptor

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1. Synthetic receptors for urea and barbiturates: An overview;Coordination Chemistry Reviews;2024-10

2. Efficient synthesis of new 17-, 18-, 19- and 20-membered N2O2-donor macrocycles by NaBH4 reduction and metal picrate extraction studies;Journal of Inclusion Phenomena and Macrocyclic Chemistry;2020-03-19

3. Barbituric acids as a useful tool for the construction of coordination and supramolecular compounds;Coordination Chemistry Reviews;2014-04

4. Insight into the multicomponent reaction mechanisms of prop-2-en-1-amine and ethyl propiolate with alloxan derivative: A density functional theory study;Chemical Physics Letters;2010-07

5. Lipid Membrane Adhesion and Fusion Driven by Designed, Minimally Multivalent Hydrogen-Bonding Lipids;Journal of the American Chemical Society;2009-10-30

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