59790-95-3

Upstream product

• 2700-22-3 Benzylidenemalononitrile 
• 100-52-7 benzaldehyde 
• 96-09-3 styrene oxide 
• 109-77-3 malononitrile 
• 1674-30-2 1-phenyl-2-chloroethanol 

Downstream Products

• 133036-79-0 2-acetamido-4,5-dihydro-4-phenyl-3-furancarbonitrile 
• 203569-66-8 4-Phenyl-2-piperidin-1-yl-4,5-dihydro-furan-3-carbonitrile 
• 486430-10-8 tetrahydro-2-imino-3-(3-oxobutyl)-4-phenyl-3-furancarbonitrile 
• 34884-15-6 2-amino-4,5-dihydro-4-phenyl-3-furancarboxamide 
• 34971-29-4 methyl tetrahydro-2-oxo-4-phenyl-3-furancarboxylate 
• 474095-36-8 methyl 2-amino-4,5-dihydro-4-phenyl-3-furancarboxylate 
• 474095-32-4 3-diaminomethylene-4,5-dihydro-4-phenyl-2(3H)-furanone 
• 474095-35-7 N-benzoyl-tetrahydro-2-oxo-4-phenyl-3-furancarboxamide 
• 474095-38-0 2-benzylamino-4,5-dihydro-4-phenyl-3-furancarboxamide 
• 474095-34-6 3-(amino-(benzamido)-methylene)-4,5-dihydro-4-phenyl-2(3H)-furanone 
• 72982-21-9 2-amino-4-phenylfuran-3-carbonitrile 
• 98061-58-6 2-benzamido-3-cyano-4-phenyl-4,5-dihydrofuran 
• 98061-63-3 2-banzamido-5-bromo-3-cyano-4-phenylfuran 
• 98061-64-4 2-benzamido-3-cyano-4-phenylfuran 

Relevant academic research and scientific papers

Controllable one-pot synthesis for scaffold diversity: Via visible-light photoredox-catalyzed Giese reaction and further transformation

This study presents a controllable one-pot synthesis for constructing valuable scaffolds (alcohols, 2,3-dihydrofurans, α-cyano-γ-butyrolactones, and γ-butyrolactones) via a visible-light photoredox-catalyzed Giese reaction and further transformation. This

Eosin Y as a Direct Hydrogen-Atom Transfer Photocatalyst for the Functionalization of C?H Bonds

Eosin Y, a well-known economical alternative to metal catalysts in visible-light-driven single-electron transfer-based organic transformations, can behave as an effective direct hydrogen-atom transfer catalyst for C?H activation. Using the alkylation of C?H bonds with electron-deficient alkenes as a model study revealed an extremely broad substrate scope, enabling easy access to a variety of important synthons. This eosin Y-based photocatalytic hydrogen-atom transfer strategy is promising for diverse functionalization of a wide range of native C?H bonds in a green and sustainable manner.

Studies on Heterocyclic Enaminonitriles. VI. Synthesis of 2-Amino-3-cyano-4,5-dihydrofurans

Malononitrile reacts with 2-chloroethanol and 1-chloro-2-propanol (or 2-methyloxirane) in the presence of sodium ethoxide to give 2-amino-3-cyano-4,5-dihydrofuran (Ia) and 2-amino-3-cyano-5-methyl-4,5-dihydrofuran (Ib), respectively.The reaction of malono