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Catalytic Asymmetric Synthesis of Enantioenriched Heterocycles Bearing a CCF3 Stereogenic Center
YY Huang, X Yang, Z Chen, F Verpoort… - … –A European Journal, 2015 - Wiley Online Library
Given the important agricultural and medicinal application of optically pure heterocycles
bearing a trifluoromethyl group at the stereogenic carbon center in the heterocyclic …
bearing a trifluoromethyl group at the stereogenic carbon center in the heterocyclic …
Catalytic enantioselective isocyanide‐based reactions: Beyond passerini and ugi multicomponent reactions
J Luo, GS Chen, SJ Chen, ZD Li… - Chemistry–A European …, 2021 - Wiley Online Library
The development of catalytic enantioselective isocyanide‐based reactions is currently of
great interest because the resulting products are valuable in organic synthesis …
great interest because the resulting products are valuable in organic synthesis …
An efficient and one-pot synthesis of imidazolines and benzimidazoles via anaerobic oxidation of carbon–nitrogen bonds in water
P Gogoi, D Konwar - Tetrahedron letters, 2006 - Elsevier
An efficient and one-pot synthesis of imidazolines and benzimidazoles via anaerobic oxidation
of carbon–nitrogen bonds in water - ScienceDirect Skip to main contentSkip to article Elsevier …
of carbon–nitrogen bonds in water - ScienceDirect Skip to main contentSkip to article Elsevier …
Preparation of bio-inspired trimethoxysilyl group terminated poly (1-vinylimidazole)-modified-chitosan composite for adsorption of chromium (VI) ions
Abstract Chitosan and poly (1-vinylimidazole) are both potential adsorbents to remove Cr
(VI). Here, we designed the preparation of new adsorbents by combining chitosan and poly …
(VI). Here, we designed the preparation of new adsorbents by combining chitosan and poly …
Multicomponent synthesis of 2-imidazolines
RS Bon, B van Vliet, NE Sprenkels… - The Journal of …, 2005 - ACS Publications
A multicomponent reaction (MCR) between amines, aldehydes, and isocyanides bearing an
acidic α-proton gives easy access to a diverse range of highly substituted 2-imidazolines …
acidic α-proton gives easy access to a diverse range of highly substituted 2-imidazolines …
Direct Catalytic Enantio‐and Diastereoselective Mannich Reaction of Isocyanoacetates and Ketimines
A catalytic asymmetric synthesis of imidazolines with a fully substituted β‐carbon atom by a
Mannich‐type addition/cyclization reaction of isocyanoacetate pronucleophiles and N …
Mannich‐type addition/cyclization reaction of isocyanoacetate pronucleophiles and N …
Novel multicomponent reaction for the combinatorial synthesis of 2-imidazolines
RS Bon, C Hong, MJ Bouma, RF Schmitz… - Organic …, 2003 - ACS Publications
Novel Multicomponent Reaction for the Combinatorial Synthesis of 2-Imidazolines | Organic
Letters Recently Viewedclose modal ACS ACS Publications C&EN CAS Find my institution Log …
Letters Recently Viewedclose modal ACS ACS Publications C&EN CAS Find my institution Log …
A mild and efficient one-pot synthesis of 2-dihydroimidazoles from aldehydes
H Fujioka, K Murai, Y Ohba, A Hiramatsu, Y Kita - Tetrahedron letters, 2005 - Elsevier
A mild and efficient one-pot synthesis of 2-dihydroimidazoles from aldehydes - ScienceDirect
Skip to main contentSkip to article Elsevier logo Journals & Books Search RegisterSign in …
Skip to main contentSkip to article Elsevier logo Journals & Books Search RegisterSign in …
Direct Asymmetric Mannich‐Type Reaction of α‐Isocyanoacetates with Ketimines using Cinchona Alkaloid/Copper (II) Catalysts
M Hayashi, M Iwanaga, N Shiomi… - Angewandte Chemie …, 2014 - Wiley Online Library
The enantioselective direct Mannich‐type reaction of ketimines with α‐isocyanoacetates has
been developed. Excellent yields and enantioselectivity were observed for the reaction of …
been developed. Excellent yields and enantioselectivity were observed for the reaction of …
Catalytic synthesis of N‐unprotected piperazines, morpholines, and thiomorpholines from aldehydes and SnAP reagents
MU Luescher, JW Bode - Angewandte Chemie, 2015 - Wiley Online Library
Commercially available SnAP (stannyl amine protocol) reagents allow the transformation of
aldehydes and ketones into a variety of N‐unprotected heterocycles. By identifying new …
aldehydes and ketones into a variety of N‐unprotected heterocycles. By identifying new …