Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Amol M. Kendhale"'
Publikováno v:
Angewandte Chemie International Edition. 49:1778-1781
Publikováno v:
Tetrahedron Letters. 49:3056-3059
This Letter reports the utility of a heavily constrained cis-fused bicyclo[3.3.0]octane (octahydropentalene) aliphatic template for effecting molecular self-assembly. An attractive feature of this system is its heavily constrained alicyclic backbone
Autor:
Christopher, Menelaou, Jeroen, ter Schiphorst, Amol M, Kendhale, Patrick, Parkinson, Michael G, Debije, Albertus P H J, Schenning, Laura M, Herz
Publikováno v:
The journal of physical chemistry letters. 6(7)
Materials showing rapid intramolecular energy transfer and polarization switching are of interest for both their fundamental photophysics and potential for use in real-world applications. Here, we report two donor-acceptor-donor triad dyes based on p
Autor:
Brice Kauffmann, Katta Laxmi-Reddy, Ivan Huc, Yann Ferrand, Amol M. Kendhale, Zeyuan Dong, Legiso Poniman
Publikováno v:
The Journal of organic chemistry. 76(1)
The synthesis of quinoline-derived helically folded aromatic oligoamides functionalized by various chiral functions at their N-terminus is reported. When a (1S)-(−)-camphanyl moiety was introduced, it was found that helix handedness was completely
Autor:
Arup Roy, Vedavati G. Puranik, Rajesh G. Gonnade, Panchami Prabhakaran, Kuruppanthara N. Vijayadas, Gangadhar J. Sanjayan, Amol M. Kendhale, Veera V. E. Ramesh
Publikováno v:
Organicbiomolecular chemistry. 9(2)
This communication describes the development of conformationally constrained unnatural aromatic amino acids, constructed on rigid backbone wherein the carboxyl and amino groups project in two dimensions (planes) on the aromatic framework. Such a feat
Autor:
Amol M. Kendhale, Cécile Marie, Muriel Pipelier, Ivan Huc, Didier Dubreuil, Brice Kauffmann, Virginie Blot, Axelle Grélard, Yann Ferrand
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2010, 132 (23), pp.7858+. ⟨10.1021/ja102794a⟩
Journal of the American Chemical Society, 2010, 132 (23), pp.7858+. ⟨10.1021/ja102794a⟩
Journal of the American Chemical Society, American Chemical Society, 2010, 132 (23), pp.7858+. ⟨10.1021/ja102794a⟩
Journal of the American Chemical Society, 2010, 132 (23), pp.7858+. ⟨10.1021/ja102794a⟩
A helical aromatic oligoamide foldamer encapsulates tartaric acid with exceptional affinity, selectivity, and diastereoselectivity. The structure of the complex has been elucidated both in solution by NMR spectroscopy and in the solid state by X-ray
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39bf80ed33eb667f0ff8438ce1140cac
https://hal.archives-ouvertes.fr/hal-02143497
https://hal.archives-ouvertes.fr/hal-02143497
Autor:
Pattuparambil R. Rajamohanan, Rajesh G. Gonnade, Gangadhar J. Sanjayan, Amol M. Kendhale, Hans-Jörg Hofmann
Publikováno v:
Chemical communications (Cambridge, England). (22)
This communication demonstrates the utility of inherently rigid building blocks such as 1,1'-spirobi(indane) for generating conformationally ordered synthetic oligomers with structural architectures distinct from those classically observed.
Publikováno v:
Acta Crystallographica Section E: Structure Reports
In the molecule of the title compound, C(18)H(32)N(2)O(4), the central bicyclo-[3.3.0]octane (octa-hydro-penta-lene) has a rigid ring junction. Both rings of the bicyclo-[3.3.0]octane unit adopt an envelope conformation, and the flexible tert-butyl-c
Publikováno v:
Chemical communications (Cambridge, England). (26)
Herein we present the first unequivocal evidence of the ability of isotactic N-alkyl acrylamide oligomers to assume self-assembled sheet-like structures that are reminiscent of protein beta-sheets.
Publikováno v:
New Journal of Chemistry. 32:909
This letter describes an efficient tandem non-polymerization strategy to deliver higher order N-acrylamide oligomers. These oligomers, accessible in an one-pot procedure, are potential intermediates for the correlation of stereochemistry (tacticity)