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Synthesis, ISSN 0039-7881, 03/2017, Volume 49, Issue 6, pp. 1223 - 1230
Abstract Various representative copper(I)-exchanged zeolites were investigated for their catalytic potential in Chan–Lam cross-coupling reactions. Cu I -USY... 
paper | cross-coupling | copper | C-N bond formation | zeolites | heterogeneous catalysis | Chan-Lam reaction
Journal Article
SYNTHESIS-STUTTGART, ISSN 0039-7881, 03/2017, Volume 49, Issue 6, pp. 1223 - 1230
Various representative copper(I)-exchanged zeolites were investigated for their catalytic potential in Chan-Lam cross-coupling reactions. Cu-I-USY appeared as... 
CUPRIC ACETATE | C-N bond formation | heterogeneous catalysis | CLICK CHEMISTRY | ARYLATION | CHEMISTRY, ORGANIC | IMIDAZOLES | ARYLBORONIC ACIDS | PHENYL | BORONIC ACIDS | DIARYL ETHER SYNTHESIS | zeolites | AMINES | cross-coupling | copper | Chan-Lam reaction
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 06/2018, Volume 83, Issue 12, pp. 6408 - 6422
The copper(I)-doped zeolite Cu-I-USY proved to be a versatile, efficient, and recyclable catalyst for various Ullmann-type coupling reactions. Easy to prepare... 
ORGANIC-SYNTHESIS | CROSS-COUPLING REACTIONS | COPPER NANOPARTICLES | GREEN CATALYSTS | PALLADIUM COMPLEXES | CLICK CHEMISTRY | ARYL HALIDES | CHEMISTRY, ORGANIC | BOND FORMATION | HETEROGENEOUS CATALYST | HIGHLY EFFICIENT
Journal Article
Current medicinal chemistry, ISSN 0929-8673, 11/2004, Volume 11, Issue 21, p. 2799
Numerous backbone constraints can be used to develop pseudopeptides or pseudomimetics of biologically active peptides. Among those, N- and Calpha-methyl amino... 
Amino Acids - metabolism | Animals | Peptides - chemical synthesis | Peptides - metabolism | Peptides - chemistry | Humans | Amino Acids - chemistry | Molecular Structure | Amino Acids - chemical synthesis | Methylation
Journal Article
Current Medicinal Chemistry, ISSN 0929-8673, 11/2004, Volume 11, Issue 21, p. 2799
  Numerous backbone constraints can be used to develop pseudopeptides or pseudomimetics of biologically active peptides. Among those, N- and Calpha-methyl... 
Journal Article
MAGNETIC RESONANCE IN CHEMISTRY, ISSN 0749-1581, 10/2008, Volume 46, Issue 10, pp. 918 - 924
Ability of N,N'-linked oligoureas containing proteinogenic side chains to adopt a stable helix conformation in solution has been described recently. NMR as... 
structure calculation | oligoureas | ACIDS | N,N'-LINKED OLIGOUREAS | NUCLEAR-MAGNETIC-RESONANCE | SECONDARY STRUCTURES | C-13 natural abundance | CHEMISTRY, PHYSICAL | BETA-PEPTIDES | CHEMISTRY, MULTIDISCIPLINARY | foldamers | SIDE-CHAINS | NMR | WATER SATURATION | CIRCULAR-DICHROISM | SPECTROSCOPY | scalar couplings | DIPOLAR COUPLINGS | peptidomimetics | HSQC | spin state selection | methylene
Journal Article
Current Medicinal Chemistry, ISSN 0929-8673, 01/2004, Volume 11, Issue 21, pp. 2799 - 2822
Numerous backbone constraints can be used to develop pseudopeptides or pseudomimetics of biologically active peptides. Among those, N- and C alpha - methyl... 
Journal Article
Genome Medicine, ISSN 1756-994X, 01/2018, Volume 10, Issue 1, pp. 1 - 13
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2012, Volume 7, Issue 9, p. e44328
Journal Article
Clinical Genetics, ISSN 0009-9163, 05/2016, Volume 89, Issue 5, pp. 630 - 635
Journal Article
by Karolak, Justyna A and Vincent, Marie and Deutsch, Gail and Gambin, Tomasz and Cogné, Benjamin and Pichon, Olivier and Vetrini, Francesco and Mefford, Heather C and Dines, Jennifer N and Golden-Grant, Katie and Dipple, Katrina and Freed, Amanda S and Leppig, Kathleen A and Dishop, Megan and Mowat, David and Bennetts, Bruce and Gifford, Andrew J and Weber, Martin A and Lee, Anna F and Boerkoel, Cornelius F and Bartell, Tina M and Ward-Melver, Catherine and Besnard, Thomas and Petit, Florence and Bache, Iben and Tümer, Zeynep and Denis-Musquer, Marie and Joubert, Madeleine and Martinovic, Jelena and Bénéteau, Claire and Molin, Arnaud and Carles, Dominique and André, Gwenaelle and Bieth, Eric and Chassaing, Nicolas and Devisme, Louise and Chalabreysse, Lara and Pasquier, Laurent and Secq, Véronique and Don, Massimiliano and Orsaria, Maria and Missirian, Chantal and Mortreux, Jérémie and Sanlaville, Damien and Pons, Linda and Küry, Sébastien and Bézieau, Stéphane and Liet, Jean-Michel and Joram, Nicolas and Bihouée, Tiphaine and Scott, Daryl A and Brown, Chester W and Scaglia, Fernando and Tsai, Anne Chun-Hui and Grange, Dorothy K and Phillips, John A and Pfotenhauer, Jean P and Jhangiani, Shalini N and Gonzaga-Jauregui, Claudia G and Chung, Wendy K and Schauer, Galen M and Lipson, Mark H and Mercer, Catherine L and van Haeringen, Arie and Liu, Qian and Popek, Edwina and Coban Akdemir, Zeynep H and Lupski, James R and Szafranski, Przemyslaw and Isidor, Bertrand and Le Caignec, Cedric and Stankiewicz, Paweł
The American Journal of Human Genetics, ISSN 0002-9297, 02/2019, Volume 104, Issue 2, pp. 213 - 228
Journal Article