Results 91 to 100 of about 8,155 (194)

New approaches to organocatalysis based on C–H and C–X bonding for electrophilic substrate activation

open access: yesBeilstein Journal of Organic Chemistry, 2016
Hydrogen bond donor catalysis represents a rapidly growing subfield of organocatalysis. While traditional hydrogen bond donors containing N–H and O–H moieties have been effectively used for electrophile activation, activation based on other types of non ...
Pavel Nagorny, Zhankui Sun
doaj   +1 more source

Chiral benzylamines in organocatalysis

open access: yes, 2011
Hirālie benzilamīni organokatalīzē. Kalniņš T., zinātniskais vadītājs Dr. ķīm., asoc. prof. Sūna E. Bakalaura darbs, 84 lappuses, 42 attēli, 9 tabulas, 65 literatūras avoti. Latviešu valodā.
Kalniņš, Toms
core  

Enantioselective α-heterofunctionalization reactions of catalytically generated C1-Lewis base enolates

open access: yesTetrahedron Chem
Chiral Lewis base (LB) organocatalysis has emerged as a powerful covalent catalysis concept which allows for highly selective asymmetric C–C and C-heteroatom bond formations.
Magdalena Piringer   +5 more
doaj   +1 more source

Asymmetric synthesis of tetrahydroquinolines through supramolecular organocatalysis

open access: yes, 2014
Functionalized chiral tetrahydroquinolines were synthesized through supramolecular organocatalysis using quinidine-NH-thiourea 3c/L-phenylalanine 4i followed by reductive amination from the simple ...
Ramachary, Dhevalapally B.   +1 more
core   +1 more source

Computational Strategies for Designing Bidentate Hypervalent Iodine Catalysts in Halogen Bond-Mediated Organocatalysis

open access: yes
<p>Computational Strategies for Designing Bidentate Hypervalent Iodine Catalysts in Halogen Bond-Mediated Organocatalysis</p> <p>Email: cristina.trujillodelvalle@manchester.ac.uk</p> <p> </p> <p>Please find ...
Lee, Rico Shing   +4 more
core   +2 more sources

Cross-trienamines in Asymmetric Organocatalysis

open access: yes, 2015
Cross-conjugated trienamines are introduced as a new concept in asymmetric organocatalysis. These intermediates are applied in highly enantioselective Diels–Alder and addition reactions, providing functionalized bicyclo[2.2.2]­octane compounds and γ ...
Karl Anker Jørgensen (1287900)   +5 more
core   +2 more sources

Organocatalysis [PDF]

open access: yesAnnual Reports Section "B" (Organic Chemistry), 2011
S. Hata, M. P. Sibi
openaire   +2 more sources

Synthesis of Polyurethanes Using Organocatalysis: A Perspective

open access: yes, 2015
Organocatalysis has become an invaluable tool for polymer synthesis, and its utility has been demonstrated in ring-opening, anionic, zwitterionic, and group-transfer polymerizations.
Haritz Sardon   +11 more
core   +1 more source

Targeting a key protein-protein interaction surface on mitogen-activated protein kinases by a precision-guided warhead scaffold

open access: yesNature Communications
For mitogen-activated protein kinases (MAPKs) a shallow surface—distinct from the substrate binding pocket—called the D(ocking)-groove governs partner protein binding.
Ádám Levente Póti   +17 more
doaj   +1 more source

Searching for untrodden paths in organocatalysis territory

open access: yes, 2010
In spite of the tremendous growth experienced by the field of asymmetric organocatalysis in the last decade, it is important to realize that we are still far away from having explored all of the possible pathways in organocatalysis ‘territory'; the ...
Xavier Companyó   +12 more
core   +1 more source

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