120 results on '"Fan, Xue‐Sen"'
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2. Microwave-Promoted Metal-Free α-Alkylation of Ketones with Cycloalkanes through Cross-Coupling of C(sp3 )−H Bonds
3. Synthesis of cyclopentenyl and cyclohexenyl ketones via [3 + 2] and [4 + 2] annulations of 1,2-allenic ketones
4. Synthesis of 4-Oxo-but-2-enals throughtBuONO and TEMPO-Promoted Cascade Reactions of Homoallylic Alcohols
5. Bu4NI-Catalyzed andtBuOOH-Oxidized Esterification of Aldehydes with Alkyl Halides in Water
6. ChemInform Abstract: One‐Pot Sequential Reactions Featuring a Copper‐Catalyzed Amination Leading to Pyrido[2′,1′:2,3]imidazo[4,5‐c]quinolines and Dihydropyrido[2′,1′:2,3]imidazo[4,5‐c]quinolines.
7. ChemInform Abstract: Synthesis of 2‐Aminoquinoline‐3‐carboamides and Pyrimido[4,5‐b]quinolin‐4‐ones Through Copper‐Catalyzed One‐Pot Multicomponent Reactions.
8. Copper-catalyzed tandem reaction of 2-bromobenzyl bromides with 1,3-dicarbonyl compounds leading to 4H-chromenes
9. One-pot Sequential Reactions Featuring a Copper-catalyzed Amination Leading to Pyrido[2′,1′:2,3]imidazo[4,5-c]quinolines and Dihydropyrido[2′,1′:2,3]imidazo[4,5-c]quinolines
10. Synthesis of 1,2-allenic ketones through oxidation of homopropargyl alcohols with CrO 3(cat.)/TBHP under MWI
11. Microwave-Promoted Metal-Free α-Alkylation of Ketones with Cycloalkanes through Cross-Coupling of C(sp3)−H Bonds.
12. Synthesis of 4-Oxo-but-2-enals through tBuONO and TEMPO-Promoted Cascade Reactions of Homoallylic Alcohols.
13. Bu4NI-Catalyzed and tBuOOH-Oxidized Esterification of Aldehydes with Alkyl Halides in Water.
14. An efficient and green preparation of 5-aminophosphonate substituted pyrimidine nucleosides under solvent-free conditions
15. Synthesis of 2-Aminoquinoline-3-carboamides and Pyrimido[4,5-b]quinolin-4-ones through Copper-Catalyzed One-pot Multicomponent Reactions
16. ChemInform Abstract: Environmentally Sustainable and Chemoselectively Favorable Synthesis of Substituted 2H‐Pyran‐2‐ones in Water under MWI.
17. ChemInform Abstract: Synthesis of Cyclopentenyl and Cyclohexenyl Ketones via [3 + 2] and [4 + 2] Annulations of 1,2-Allenic Ketones
18. Synthesis of cyclopentenyl and cyclohexenyl ketones via [3+2] and [4+2] annulations of 1,2-allenic ketones
19. Preparation of nucleoside–pyridine hybrids and pyridine attached acylureas from an unexpected uracil ring-opening and pyridine ring-forming sequence
20. Synthesis of fused pyran and arylbis(4-hydroxy-6-methyl-2-oxo-2 H-pyran-3-yl)methane in ionic liquid
21. Environmentally Sustainable and Chemo-selectively Favorable Synthesis of Substituted 2H-Pyran-2-ones in Water under MWI
22. ChemInform Abstract: Iodine-Initiated Domino Reaction of Hepta-1,2,-dien-6-yn-4-ols and Broensted Acid Promoted Cyclization of Hepta-1,2,6-trien-4-ols Leading to Functionalized Benzenes.
23. 3,4-Dihydro-1H-benzo[c]chromene-1,6(2H)-dione
24. ChemInform Abstract: Copper-Catalyzed Tandem Reaction of 2-Bromobenzyl Bromides with 1,3-Dicarbonyl Compounds Leading to 4H-Chromenes.
25. Iodine-Initiated Domino Reaction of Hepta-1,2-dien-6-yn-4-ols and Brønsted Acid Promoted Cyclization of Hepta-1,2,6-trien-4-ols Leading to Functionalized Benzenes
26. A novel synthesis of pyrazolo[3,4- b]pyridine derivatives through multi-component reaction in ionic liquid
27. An unexpected reaction of cyanothioacetamide: Novel preparation of pyrazolo[3,4- b]-pyridine derivatives under MWI
28. 5,6-Dimethyl-4-phenyl-2H-pyran-2-one
29. Microwave‐Promoted Metal‐Free α‐Alkylation of Ketones with Cycloalkanes through Cross‐Coupling of C(sp3)−H Bonds
30. ChemInform Abstract: Synthesis of 1,2-Allenic Ketones Through Oxidation of Homopropargyl Alcohols with CrO3(cat.)/TBHP under MWI.
31. Synthesis of 1,2-allenic ketones through oxidation of homopropargyl alcohols with CrO3(cat.)/TBHP under MWI
32. Reductive Cyclodimerization of α, β- Unsaturated Ketones Promoted by AlCl3/Sm System: A Facile Synthesis of 2-Aroyl-1,3,4-triaryl Cyclopentanol Derivatives
33. A Simple Access to Chalcones via Modified Mukaiyama Aldol Condensation Promoted by SmI3/TMSCl
34. ChemInform Abstract: Synthesis of Fused Pyran and Arylbis(4‐hydroxy‐6‐methyl‐2‐oxo‐2H‐pyran‐3‐yl)methane in Ionic Liquid.
35. ChemInform Abstract: Novel and Efficient Synthesis of Pyrazolo[3,4‐b]pyridin‐6‐ones or Their Hydrogenated Derivatives Through One‐Pot Reaction in Ionic Liquid.
36. ChemInform Abstract: An Alternative Preparation of Pyrazolo-Pyridine Derivatives in Ionic Liquid and Comparison Study on the Reactivity of Thioamide and Amide Group.
37. Synthesis of fused pyran and arylbis(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)methane in ionic liquid
38. Novel and Efficient Synthesis of Pyrazolo[3,4-b]pyridin-6-ones or Their Hydrogenated Derivatives through One-Pot Reaction in Ionic Liquid
39. ChemInform Abstract: An Unexpected Reaction of Cyanothioacetamide: Novel Preparation of Pyrazolo[3,4-b]pyridine Derivatives under MWI.
40. 4-(4-Bromophenyl)-4,5,6,7-tetrahydro-3-methyl-6-oxo-1-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile ethanol solvate
41. 6,7-Dihydro-4-(4-methoxyphenyl)-3-methyl-6-oxo-1-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile
42. ChemInform Abstract: A Novel Synthesis of Pyrazolo[3,4‐b]pyridine Derivatives Through Multicomponent Reaction in Ionic Liquid.
43. ChemInform Abstract: Novel Synthesis of meso‐Tetraarylporphyrins by Using I2 as Catalyst and Air as Oxidant under Thermal or UV Conditions.
44. 2-[(5-Amino-3-methyl-1-phenyl-1H-pyrazol-4-yl)(4-chlorophenyl)methyl]malononitrile
45. 6-Amino-3-methyl-4-(4-nitrophenyl)-1-phenylpyrazolo[3,4-b]pyridine-5-carbonitrile
46. Novel Synthesis ofmeso-Tetraarylporphyrins by Using I2as Catalyst and Air as Oxidant under Thermal or UV Conditions
47. An Alternative Preparation of Pyrazolo-pyridine Derivatives in Ionic Liquid and Comparison Study on the Reactivity of Thioamide and Amide Group
48. Solvent‐Free Synthesis of 5‐Oxo‐5,6,7,8‐tetrahydro‐4H‐benzo‐[b]‐pyran Derivatives under Microwave Irradiation.
49. Synthesis of 2-Aminoquinoline-3-carboamides and Pyrimido[4,5-b]quinolin-4-ones through Copper-Catalyzed One-pot Multicomponent Reactions.
50. An Efficient and Green Synthesis of 1,4‐Dihydropyridine Derivatives Through Multi‐Component Reaction in Ionic Liquid.
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