| Year |
Citation |
Score |
| 2023 |
Jie J, Yang H, Zhao Y, Fu H. Development of diverse adjustable axially chiral biphenyl ligands and catalysts. Iscience. 26: 106344. PMID 36994080 DOI: 10.1016/j.isci.2023.106344 |
0.306 |
|
| 2021 |
Li Y, Jie J, Li H, Yang H, Fu H. Synthesis of Spirotetrahydrofuran Oxindoles via Palladium-Catalyzed [4 + 1] Cycloaddition of Diphenyl 2-Oxoindolin-3-yl Phosphates and 2-Methylidenetrimethylene Carbonate. Organic Letters. PMID 34342464 DOI: 10.1021/acs.orglett.1c02306 |
0.306 |
|
| 2021 |
Man N, Li Y, Jie J, Li H, Yang H, Zhao Y, Fu H. Synthesis of Chiral Propargylamines, Chiral 1,2-Dihydronaphtho[2,1-b]furans and Naphtho[2,1-b]furans with C-Alkynyl N,N'-Di-(tert-Butoxycarbonyl)-Aminals and β-Naphthols. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34133047 DOI: 10.1002/chem.202102040 |
0.316 |
|
| 2020 |
Yuan X, Wu X, Peng F, Yang H, Zhu C, Fu H. Organocatalytic asymmetric synthesis of arylindolyl indolin-3-ones with both axial and central chirality. Chemical Communications (Cambridge, England). PMID 32960194 DOI: 10.1039/D0Cc05432A |
0.489 |
|
| 2020 |
Man N, Lou Z, Li Y, Yang H, Zhao Y, Fu H. Organocatalytic Atroposelective Construction of Axially Chiral -Aryl Benzimidazoles Involving Carbon-Carbon Bond Cleavage. Organic Letters. PMID 32806186 DOI: 10.1021/Acs.Orglett.0C02214 |
0.447 |
|
| 2020 |
Zhu X, Liu Y, Liu C, Yang H, Fu H. Light and oxygen-enabled sodium trifluoromethanesulfinate-mediated selective oxidation of C–H bonds Green Chemistry. 22: 4357-4363. DOI: 10.1039/D0Gc00383B |
0.373 |
|
| 2019 |
Liu C, Yang H, Zhu C, Fu H. 1-Alkyl-3-alkylindolin-2-imine hydrochlorides as useful building blocks in the copper-catalyzed synthesis of polycyclic indoline scaffolds. Rsc Advances. 9: 8369-8372. PMID 35518700 DOI: 10.1039/c9ra00995g |
0.414 |
|
| 2019 |
Li Y, Lou Z, Li H, Yang H, Zhao Y, Fu H. Both Bioorthogonal Ligations and Cleavages via Reactions of Chloroquinoxalines with ortho-Dithiophenols. Angewandte Chemie (International Ed. in English). PMID 31868279 DOI: 10.1002/Anie.201913620 |
0.36 |
|
| 2019 |
Tian H, Peng F, Zhang P, Yang H, Fu H. Highly Enantioselective Iridium-Catalyzed Cascade Double Allylation Strategy: Synthesis of Pyrrolidinoindolines with an All-Carbon Quaternary Stereocenter. Organic Letters. PMID 31591895 DOI: 10.1021/Acs.Orglett.9B03382 |
0.465 |
|
| 2019 |
Wu X, Yuan X, Yang H, Fu H. Chiral Phosphoric Acid Catalyzed Asymmetric Addition of 2-(Vinyloxy)ethanol to Imines and Applications of the Products. Organic Letters. PMID 31247765 DOI: 10.1021/Acs.Orglett.9B01970 |
0.427 |
|
| 2019 |
Peng F, Tian H, Zhang P, Yang H, Fu H. Iridium-catalyzed intramolecular enantioselective allylation of quinazolin-4(3H)-one derivatives. Organic & Biomolecular Chemistry. PMID 31218327 DOI: 10.1039/C9Ob01057B |
0.471 |
|
| 2019 |
Liu C, Zhu X, Han Y, Yang H, Zhu C, Fu H. Superbase-promoted selective carbon-carbon bond cleavage driven by aromatization. Organic & Biomolecular Chemistry. PMID 31066430 DOI: 10.1039/C9Ob00606K |
0.323 |
|
| 2019 |
Yuan X, Wu X, Zhang P, Peng F, Liu C, Yang H, Zhu C, Fu H. Axially Chiral Cyclic Phosphoric Acid Enabled Enantioselective Sequential Additions. Organic Letters. PMID 30942603 DOI: 10.1021/Acs.Orglett.8B04012 |
0.408 |
|
| 2019 |
Han Y, Jin Y, Jiang M, Yang H, Fu H. Photocatalyst-Free Visible-Light Photoredox Dearomatization of Phenol Derivatives Containing Ketoximes: An Easy Access to Spiropyrrolines. Organic Letters. PMID 30794421 DOI: 10.1021/Acs.Orglett.9B00372 |
0.352 |
|
| 2019 |
Liu C, Yang H, Zhu C, Fu H. 1-Alkyl-3-alkylindolin-2-imine hydrochlorides as useful building blocks in the copper-catalyzed synthesis of polycyclic indoline scaffolds Rsc Advances. 9: 8369-8372. DOI: 10.1039/C9Ra00995G |
0.472 |
|
| 2018 |
Liu C, Zhu X, Zhang P, Yang H, Zhu C, Fu H. Axially Chiral Cyclic Diphosphine Ligand-Enabled Palladium-Catalyzed Intramolecular Asymmetric Hydroarylation. Iscience. 10: 11-22. PMID 30496972 DOI: 10.1016/J.Isci.2018.11.018 |
0.461 |
|
| 2018 |
Jiang M, Yang H, Lefebvre Q, Su J, Fu H. Olefination of Alkyl Halides with Aldehydes by Merging Visible-Light Photoredox Catalysis and Organophosphorus Chemistry. Iscience. 6: 102-113. PMID 30240604 DOI: 10.1016/J.Isci.2018.07.011 |
0.406 |
|
| 2018 |
Fu H, Jiang M, Yang H, Jin Y, Ou L. Visible-Light-Induced Decarboxylative Iodination of Aromatic Carboxylic Acids Synlett. 29: 1572-1577. DOI: 10.1055/S-0037-1610188 |
0.44 |
|
| 2018 |
Lou Z, Man N, Yang H, Zhu C, Fu H. Copper-Catalyzed Cascade Synthesis of [1,2,4]-Triazoloquinazolinones Synlett. 29: 1395-1399. DOI: 10.1055/S-0036-1591565 |
0.513 |
|
| 2017 |
Peng F, Tian H, Zhang P, Liu C, Wu X, Yuan X, Yang H, Fu H. Iridium-Catalyzed Enantioselective Synthesis of Dihydroimidazoquinazolinones by Elaborate Tuning of Chiral Cyclic Ligands. Organic Letters. PMID 29160081 DOI: 10.1021/Acs.Orglett.7B03230 |
0.442 |
|
| 2017 |
Jin Y, Ou L, Yang H, Fu H. Visible Light-Mediated Aerobic Oxidation of N-Alkylpyridinium Salts under Organic Photocatalysis. Journal of the American Chemical Society. PMID 28937217 DOI: 10.1021/Jacs.7B07883 |
0.442 |
|
| 2017 |
Li J, Lefebvre Q, Yang H, Zhao Y, Fu H. Visible light photocatalytic decarboxylative monofluoroalkenylation of α-amino acids with gem-difluoroalkenes. Chemical Communications (Cambridge, England). PMID 28869645 DOI: 10.1039/C7Cc05758J |
0.364 |
|
| 2017 |
Tian H, Zhang P, Peng F, Yang H, Fu H. Chiral Cyclic Ligand-Enabled Iridium-Catalyzed Asymmetric Arylation of Unactivated Racemic Allylic Alcohols with Anilines. Organic Letters. PMID 28661154 DOI: 10.1021/Acs.Orglett.7B01631 |
0.428 |
|
| 2017 |
Yang J, Jiang M, Jin Y, Yang H, Fu H. Visible-Light Photoredox Difluoromethylation of Phenols and Thiophenols with Commercially Available Difluorobromoacetic Acid. Organic Letters. PMID 28480711 DOI: 10.1021/Acs.Orglett.7B01118 |
0.397 |
|
| 2017 |
Li J, Zhang P, Jiang M, Yang H, Zhao Y, Fu H. Visible Light as a Sole Requirement for Intramolecular C(sp(3))-H Imination. Organic Letters. PMID 28362098 DOI: 10.1021/Acs.Orglett.7B00533 |
0.403 |
|
| 2017 |
Zhang H, Zhang P, Jiang M, Yang H, Fu H. Merging Photoredox with Copper Catalysis: Decarboxylative Alkynylation of α-Amino Acid Derivatives. Organic Letters. PMID 28198184 DOI: 10.1021/Acs.Orglett.6B03888 |
0.49 |
|
| 2017 |
Lou Z, Yang H, Zhu C, Fu H. Copper-Catalyzed C−H Activation of Substituted Pyridines Leading to Imidazopyridine Derivatives via Self-Redox of the Substrates Asian Journal of Organic Chemistry. 6: 1551-1555. DOI: 10.1002/Ajoc.201700381 |
0.431 |
|
| 2017 |
Jin Y, Fu H. Visible‐Light Photoredox Decarboxylative Couplings Asian Journal of Organic Chemistry. 6: 368-385. DOI: 10.1002/Ajoc.201600513 |
0.403 |
|
| 2016 |
Jin Y, Yang H, Fu H. Thiophenol-Catalyzed Visible-Light Photoredox Decarboxylative Couplings of N-(Acetoxy)phthalimides. Organic Letters. 18: 6400-6403. PMID 27978669 DOI: 10.1021/Acs.Orglett.6B03300 |
0.372 |
|
| 2016 |
Jiang M, Li H, Yang H, Fu H. Room-Temperature Arylation of Thiols: Breakthrough with Aryl Chlorides. Angewandte Chemie (International Ed. in English). PMID 27933699 DOI: 10.1002/Anie.201610414 |
0.441 |
|
| 2016 |
Jin Y, Yang H, Fu H. An N-(acetoxy)phthalimide motif as a visible-light pro-photosensitizer in photoredox decarboxylative arylthiation. Chemical Communications (Cambridge, England). PMID 27739553 DOI: 10.1039/C6Cc06994K |
0.363 |
|
| 2016 |
Zhang P, Yu J, Peng F, Wu X, Jie J, Liu C, Tian H, Yang H, Fu H. Development of Axially Chiral Cyclo-Biaryldiol Ligands with Adjustable Dihedral Angles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27735100 DOI: 10.1002/Chem.201603706 |
0.345 |
|
| 2016 |
Jiang M, Yang H, Fu H. Visible-Light Photoredox Borylation of Aryl Halides and Subsequent Aerobic Oxidative Hydroxylation. Organic Letters. PMID 27690142 DOI: 10.1021/Acs.Orglett.6B02553 |
0.432 |
|
| 2016 |
Zhang H, Li H, Yang H, Fu H. Iron-Catalyzed Diastereoselective Synthesis of Unnatural Chiral Amino Acid Derivatives. Organic Letters. PMID 27367820 DOI: 10.1021/Acs.Orglett.6B01493 |
0.455 |
|
| 2016 |
Li J, Tian H, Jiang M, Yang H, Zhao Y, Fu H. Consecutive visible-light photoredox decarboxylative couplings of adipic acid active esters with alkynyl sulfones leading to cyclic compounds. Chemical Communications (Cambridge, England). PMID 27345832 DOI: 10.1039/C6Cc04386K |
0.427 |
|
| 2016 |
Jiang M, Jin Y, Yang H, Fu H. Visible-light photoredox synthesis of unnatural chiral α-amino acids. Scientific Reports. 6: 26161. PMID 27185220 DOI: 10.1038/Srep26161 |
0.412 |
|
| 2016 |
Gao C, Li J, Yu J, Yang H, Fu H. Visible-light photoredox synthesis of internal alkynes containing quaternary carbons. Chemical Communications (Cambridge, England). PMID 27181024 DOI: 10.1039/C6Cc01632D |
0.432 |
|
| 2016 |
Jiang M, Yang H, Fu H. Visible-Light Photoredox Synthesis of Chiral α-Selenoamino Acids. Organic Letters. PMID 27093481 DOI: 10.1021/Acs.Orglett.6B00489 |
0.459 |
|
| 2016 |
Jin Y, Jiang M, Wang H, Fu H. Installing amino acids and peptides on N-heterocycles under visible-light assistance. Scientific Reports. 6: 20068. PMID 26830014 DOI: 10.1038/Srep20068 |
0.406 |
|
| 2016 |
Tian H, Yang H, Zhu C, Fu H. Transition metal-free intramolecular regioselective couplings of aliphatic and aromatic C-H bonds. Scientific Reports. 6: 19931. PMID 26822836 DOI: 10.1038/Srep19931 |
0.396 |
|
| 2016 |
Yu J, Jiang M, Song Z, He T, Yang H, Fu H. Iron-Catalyzed Azidoalkylthiation of Alkenes with Trimethylsilyl Azide and 1-(Alkylthio)pyrrolidine-2,5-diones Advanced Synthesis & Catalysis. 358: 2806-2810. DOI: 10.1002/Adsc.201600133 |
0.406 |
|
| 2016 |
Tian H, Yu J, Yang H, Zhu C, Fu H. Catalyst-Free Isothiocyanatoalkylthiation of Styrenes with (Alkylthio)pyrrolidine-2,5-diones and Trimethylsilyl Isothiocyanate Advanced Synthesis & Catalysis. 358: 1794-1800. DOI: 10.1002/Adsc.201501181 |
0.411 |
|
| 2015 |
Zhang H, Wang H, Yang H, Fu H. Rhodium-catalyzed denitrogenative thioacetalization of N-sulfonyl-1,2,3-triazoles with disulfides: an entry to diverse transformation of terminal alkynes. Organic & Biomolecular Chemistry. 13: 6149-53. PMID 25927418 DOI: 10.1039/C5Ob00638D |
0.447 |
|
| 2015 |
Yu J, Gao C, Song Z, Yang H, Fu H. Metal-free oxysulfenylation of alkenes with 1-(arylthio)pyrrolidine-2,5-diones and alcohols. Organic & Biomolecular Chemistry. 13: 4846-50. PMID 25826752 DOI: 10.1039/C5Ob00252D |
0.359 |
|
| 2015 |
Shi L, Wang H, Yang H, Fu H. Iron-Catalyzed Arylsulfonylation of Activated Alkenes Synlett. 26: 688-694. DOI: 10.1055/S-0034-1379940 |
0.409 |
|
| 2015 |
Yu J, Tian H, Gao C, Yang H, Jiang Y, Fu H. Boron-Catalyzed Arylthiooxygenation of N-Allylamides: Synthesis of (Arylsulfanyl)oxazolines Synlett. 26: 676-680. DOI: 10.1055/S-0034-1378948 |
0.514 |
|
| 2015 |
Yu J, Gao C, Song Z, Yang H, Fu H. Metal-Free Oxidative C-H Amidation of N,N′-Diarylureas with PhI(OAc)2: Synthesis of Benzimidazol-2-one Derivatives European Journal of Organic Chemistry. 2015: 5869-5875. DOI: 10.1002/Ejoc.201500726 |
0.469 |
|
| 2015 |
Wang H, Qiao H, Zhang H, Yang H, Zhao Y, Fu H. Rhodium-Catalyzed Hydrosilylation Reaction ofN-Sulfonyl-1,2,3-triazoles with Triphenylsilane: Access to Diverse Compounds European Journal of Organic Chemistry. 2015: 4471-4480. DOI: 10.1002/Ejoc.201500455 |
0.473 |
|
| 2015 |
Lou Z, Wu X, Yang H, Zhu C, Fu H. Copper-Catalyzed Domino Synthesis of Benzo[4,5]imidazo[1,2-a]pyrimidin-4(10H)-ones using Cyanamide as a Building Block Advanced Synthesis & Catalysis. 357: 3961-3968. DOI: 10.1002/Adsc.201500577 |
0.504 |
|
| 2015 |
Wang H, Wang Y, Yang H, Tan C, Jiang Y, Zhao Y, Fu H. Rhodium-Catalyzed Desulfination of Sodium Arenesulfinates and Oxidative Annulation with Alkynes Advanced Synthesis & Catalysis. 357: 489-499. DOI: 10.1002/Adsc.201400930 |
0.44 |
|
| 2015 |
Tian H, Yang H, Zhu C, Fu H. Arylthiolation of Arylamine Derivatives with (Arylthio)- pyrrolidine-2,5-diones Advanced Synthesis & Catalysis. 357: 481-488. DOI: 10.1002/Adsc.201400929 |
0.422 |
|
| 2014 |
Tian H, Zhu C, Yang H, Fu H. Iron or boron-catalyzed C-H arylthiation of substituted phenols at room temperature. Chemical Communications (Cambridge, England). 50: 8875-7. PMID 24969301 DOI: 10.1039/C4Cc03600J |
0.438 |
|
| 2014 |
Shi L, Wang Y, Yang H, Fu H. Copper-catalyzed bis-arylations of alkenes leading to oxindole derivatives. Organic & Biomolecular Chemistry. 12: 4070-3. PMID 24817255 DOI: 10.1039/C4Ob00576G |
0.475 |
|
| 2014 |
Zhao J, Niu Z, Fu H, Li Y. Ligand-free hydroboration of alkynes catalyzed by heterogeneous copper powder with high efficiency. Chemical Communications (Cambridge, England). 50: 2058-60. PMID 24419329 DOI: 10.1039/C3Cc48670B |
0.42 |
|
| 2014 |
Niu L, Zhang H, Yang H, Fu H. Metal-Free Iodination of Arylboronic Acids and the Synthesis of Biaryl Derivatives Synlett. 25: 995-1000. DOI: 10.1055/S-0033-1340871 |
0.43 |
|
| 2014 |
Yang X, Shi L, Fu H. Copper-Mediated Cascade Synthesis of Diaryl Sulfones via the Sandmeyer Reaction Synlett. 25: 847-852. DOI: 10.1055/S-0033-1340736 |
0.502 |
|
| 2014 |
Jiang M, Li Y, Yang H, Zong R, Jin Y, Fu H. Metal-free UV-Vis-light-induced aerobic oxidative hydroxylation of arylboronic acids in the absence of a photosensitizer Rsc Advances. 4: 12977. DOI: 10.1039/C3Ra46516K |
0.374 |
|
| 2014 |
Tian H, Qiao H, Zhu C, Fu H. Copper-catalyzed N-arylation and aerobic oxidation: one-pot synthesis of tetrahydroisoquinolino[2,1-a]quinazolinone derivatives Rsc Adv.. 4: 2694-2704. DOI: 10.1039/C3Ra44975K |
0.493 |
|
| 2014 |
Jiang M, Yang H, Li Y, Jia Z, Fu H. Metal-free synthesis of substituted phenols from arylboronic acids in water at room temperature Chinese Chemical Letters. 25: 715-719. DOI: 10.1016/J.Cclet.2014.03.018 |
0.42 |
|
| 2014 |
Shi L, Yang X, Wang Y, Yang H, Fu H. Metal-Free Trifluoromethylation and Arylation of Alkenes: Domino Synthesis of Oxindole Derivatives Advanced Synthesis & Catalysis. 356: 1021-1028. DOI: 10.1002/Adsc.201300995 |
0.382 |
|
| 2013 |
Yu J, Jin Y, Zhang H, Yang X, Fu H. Copper-catalyzed aerobic oxidative C-H functionalization of substituted pyridines: synthesis of imidazopyridine derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 16804-8. PMID 24151176 DOI: 10.1002/Chem.201302737 |
0.467 |
|
| 2013 |
Yu J, Yang H, Jiang Y, Fu H. Copper-catalyzed aerobic oxidative C-H and C-C functionalization of 1-[2-(arylamino)aryl]ethanones leading to acridone derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 4271-7. PMID 23401330 DOI: 10.1002/Chem.201204169 |
0.369 |
|
| 2013 |
Wang F, Yang H, Fu H, Pei Z. Efficient copper-catalyzed Michael addition of acrylic derivatives with primary alcohols in the presence of base. Chemical Communications (Cambridge, England). 49: 517-9. PMID 23192281 DOI: 10.1039/C2Cc37595H |
0.387 |
|
| 2013 |
Fu H, Cheng C, Liu Q, Zhao Y. Copper-Catalyzed Sequential N-Arylation and Aerobic Oxidation: Synthesis of Quinazoline Derivatives Synlett. 24: 2089-2094. DOI: 10.1055/S-0033-1339800 |
0.497 |
|
| 2013 |
Jiang M, Yang H, Li Y, Jia Z, Fu H. Efficient ipso-nitration of arylboronic acids with iron nitrate as the nitro source Rsc Advances. 3: 25602. DOI: 10.1039/C3Ra45118F |
0.37 |
|
| 2013 |
Liu Q, Yang H, Jiang Y, Zhao Y, Fu H. General and efficient copper-catalyzed aerobic oxidative synthesis of N-fused heterocycles using amino acids as the nitrogen source Rsc Advances. 3: 15636. DOI: 10.1039/C3Ra41644E |
0.48 |
|
| 2013 |
Wang M, Jin Y, Yang H, Fu H, Hu L. Copper-catalyzed N-arylation and aerobic oxidative C–H/C–H coupling: one-pot synthesis of indoloimidazoquinoline derivatives Rsc Advances. 3: 8211-8214. DOI: 10.1039/C3Ra40999F |
0.494 |
|
| 2013 |
Shi L, Wang R, Yang H, Jiang Y, Fu H. Efficient copper-catalyzed domino synthesis of tetrazoloisoquinolines Rsc Advances. 3: 6278. DOI: 10.1039/C3Ra23230A |
0.511 |
|
| 2013 |
Lu J, Yang H, Jin Y, Jiang Y, Fu H. Easy conjugations between molecules via copper-catalyzed reactions of ortho-aromatic diamines with ketones Green Chemistry. 15: 3184. DOI: 10.1039/C3Gc41585F |
0.449 |
|
| 2013 |
Niu L, Yang H, Jiang Y, Fu H. Efficient Synthesis of Dibenzoxaborininols from Diaryl Ethers and Their Application to Dibenzofuran Synthesis Advanced Synthesis & Catalysis. 355: 3625-3632. DOI: 10.1002/Adsc.201300567 |
0.497 |
|
| 2013 |
Wang Y, Wang R, Jiang Y, Tan C, Fu H. Copper-catalyzed domino synthesis of 4-oxopyrimido[1,2-a] indole derivatives Advanced Synthesis and Catalysis. 355: 2928-2935. DOI: 10.1002/Adsc.201300475 |
0.469 |
|
| 2013 |
Liu T, Yang H, Jiang Y, Fu H. Copper-Catalyzed Selective Oxidative Acylation of Secondary Anilines with Ethyl Glyoxalate: Domino Synthesis of Indoline-2,3-diones Advanced Synthesis & Catalysis. 355: 1169-1176. DOI: 10.1002/Adsc.201300044 |
0.476 |
|
| 2013 |
Shi L, Yang H, Jiang Y, Fu H. Copper-Catalyzed C-Arylation and Denitrogenation of Tetrazoles: Domino Synthesis of 1,3-Diaminoisoquinoline Derivatives Advanced Synthesis & Catalysis. 355: 1177-1184. DOI: 10.1002/Adsc.201201022 |
0.487 |
|
| 2013 |
Lu J, Zhang H, Chen X, Liu H, Jiang Y, Fu H. Palladium‐Catalyzed Synthesis of Aromatic Ketones and Isoindolobenzimidazoles via Selective Aromatic CH Bond Acylation Advanced Synthesis & Catalysis. 355: 529-536. DOI: 10.1002/Adsc.201200743 |
0.457 |
|
| 2012 |
Xie R, Ling Y, Fu H. Copper-catalyzed synthesis of benzocarbazoles via α-C-arylation of ketones. Chemical Communications (Cambridge, England). 48: 12210-2. PMID 23146998 DOI: 10.1039/C2Cc36403D |
0.488 |
|
| 2012 |
Zhao J, Zhao Y, Fu H. K2CO3-catalyzed synthesis of chromones and 4-quinolones through the cleavage of aromatic C-O bonds. Organic Letters. 14: 2710-3. PMID 22587645 DOI: 10.1021/Ol300908G |
0.368 |
|
| 2012 |
Niu L, Yang H, Wang R, Fu H. Metal-free ortho C-H borylation of 2-phenoxypyridines under mild conditions. Organic Letters. 14: 2618-21. PMID 22548500 DOI: 10.1021/Ol300950R |
0.394 |
|
| 2012 |
Wang X, Jin Y, Zhao Y, Zhu L, Fu H. Copper-catalyzed aerobic oxidative intramolecular C-H amination leading to imidazobenzimidazole derivatives. Organic Letters. 14: 452-5. PMID 22206482 DOI: 10.1021/Ol202884Z |
0.462 |
|
| 2012 |
Fu H, Xu H, Jiang Y. Copper-Catalyzed Synthesis of 1,2,4-Triazoles via Sequential Coupling and Aerobic Oxidative Dehydrogenation of Amidines Synlett. 24: 125-129. DOI: 10.1055/S-0032-1317692 |
0.483 |
|
| 2012 |
Liu T, Fu H. Copper-Catalyzed Synthesis of N-Heterocyclic Compounds Synthesis. 44: 2805-2824. DOI: 10.1055/S-0032-1316763 |
0.463 |
|
| 2012 |
Xu W, Jiang Y, Fu H. Copper-Catalyzed Aerobic Oxidative Synthesis of Primary Amides from (Aryl)methanamines Synlett. 23: 801-804. DOI: 10.1055/S-0031-1290302 |
0.435 |
|
| 2012 |
Yang X, Jin Y, Liu H, Jiang Y, Fu H. Easy and efficient one-pot synthesis of pyrazolo[1,5-c]quinazolines under mild copper-catalyzed conditions Rsc Advances. 2: 11061. DOI: 10.1039/C2Ra21929H |
0.492 |
|
| 2012 |
Yang X, Luo Y, Jin Y, Liu H, Jiang Y, Fu H. Concise and efficient one-pot copper-catalyzed synthesis of H-pyrazolo[5,1-a]isoquinolines Rsc Advances. 2: 8258. DOI: 10.1039/C2Ra21305B |
0.483 |
|
| 2012 |
Yang X, Li S, Liu H, Jiang Y, Fu H. Domino reactions of 1-(2-alkoxyaryl)-3-akylprop-2-yn-1-ones with sodium sulfide leading to thiochromen-4-one derivatives Rsc Advances. 2: 6549. DOI: 10.1039/C2Ra20897K |
0.395 |
|
| 2012 |
Zhang H, Jin Y, Liu H, Jiang Y, Fu H. Copper‐Catalyzed Cascade Synthesis of 1H‐Indolo[1,2‐c]quinazoline Derivatives European Journal of Organic Chemistry. 2012: 6798-6803. DOI: 10.1002/Ejoc.201200953 |
0.457 |
|
| 2012 |
Liu T, Zhu C, Yang H, Fu H. Copper-Catalyzed Domino Synthesis of Isoquinolino[2,3-a]quinazolinones Advanced Synthesis & Catalysis. 354: 1579-1584. DOI: 10.1002/Adsc.201100951 |
0.508 |
|
| 2012 |
Niu L, Yang H, Yang D, Fu H. Functionalizations of Aryl CH Bonds in 2-Arylpyridines via Sequential Borylation and Copper Catalysis Advanced Synthesis & Catalysis. 354: 2211-2217. DOI: 10.1002/Adsc.201100930 |
0.377 |
|
| 2012 |
Yang D, Wang Y, Yang H, Liu T, Fu H. Copper-Catalyzed Domino Synthesis of Benzimidazo[2,1-b]quin- azolin-12(6H)-ones Using Cyanamide as a Building Block Advanced Synthesis & Catalysis. 354: 477-482. DOI: 10.1002/Adsc.201100580 |
0.455 |
|
| 2011 |
Xu H, Fu H. Copper-catalyzed one-pot synthesis of imidazo/benzoimidazoquinazolinones by sequential Ullmann-type coupling and intramolecular C-H amidation. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 1180-6. PMID 22190047 DOI: 10.1002/Chem.201102794 |
0.493 |
|
| 2011 |
Xie R, Fu H, Ling Y. Copper-catalyzed N-arylation of amines with part-per-million catalyst loadings under air at room temperature. Chemical Communications (Cambridge, England). 47: 8976-8. PMID 21727962 DOI: 10.1039/C1Cc13516C |
0.454 |
|
| 2011 |
Lu J, Jin Y, Liu H, Jiang Y, Fu H. Copper-catalyzed aerobic oxidative intramolecular alkene C-H amination leading to N-heterocycles. Organic Letters. 13: 3694-7. PMID 21696194 DOI: 10.1021/Ol2013395 |
0.472 |
|
| 2011 |
Liu T, Wang R, Yang H, Fu H. Efficient copper-catalyzed synthesis of poly-N-heterocycles containing amino acid residues. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 6765-71. PMID 21538622 DOI: 10.1002/Chem.201100690 |
0.507 |
|
| 2011 |
Lu J, Fu H. Copper-catalyzed cascade synthesis of alkyl 6-aminobenzimidazo[2,1-a]isoquinoline-5-carboxylates. The Journal of Organic Chemistry. 76: 4600-5. PMID 21520964 DOI: 10.1021/Jo200508Q |
0.541 |
|
| 2011 |
Yang H, Li Y, Jiang M, Wang J, Fu H. General copper-catalyzed transformations of functional groups from arylboronic acids in water. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 5652-60. PMID 21480407 DOI: 10.1002/Chem.201003711 |
0.4 |
|
| 2011 |
Xu W, Fu H. Amino acids as the nitrogen-containing motifs in copper-catalyzed domino synthesis of N-heterocycles. The Journal of Organic Chemistry. 76: 3846-52. PMID 21469687 DOI: 10.1021/Jo2002227 |
0.483 |
|
| 2011 |
Xu S, Lu J, Fu H. Copper-catalyzed cascade synthesis of benzimidazoquinazoline derivatives under mild condition. Chemical Communications (Cambridge, England). 47: 5596-8. PMID 21455510 DOI: 10.1039/C1Cc10383K |
0.501 |
|
| 2011 |
Zhao J, Zhao Y, Fu H. Transition-metal-free intramolecular Ullmann-type O-arylation: synthesis of chromone derivatives. Angewandte Chemie (International Ed. in English). 50: 3769-73. PMID 21416568 DOI: 10.1002/Anie.201007302 |
0.473 |
|
| 2011 |
Xu W, Jin Y, Liu H, Jiang Y, Fu H. Copper-catalyzed domino synthesis of quinazolinones via Ullmann-type coupling and aerobic oxidative C-H amidation. Organic Letters. 13: 1274-7. PMID 21344914 DOI: 10.1021/ol1030266 |
0.333 |
|
| 2011 |
Yang D, Yang H, Fu H. Copper-catalyzed aerobic oxidative synthesis of aromatic carboxylic acids. Chemical Communications (Cambridge, England). 47: 2348-50. PMID 21152586 DOI: 10.1039/C0Cc04319B |
0.508 |
|
| 2011 |
Chen L, Fu H, Qiao R. Efficient copper-catalyzed synthesis of fused pyridoquinazolones Synlett. 1930-1936. DOI: 10.1055/S-0030-1260968 |
0.471 |
|
| 2011 |
Yang D, Li B, Yang H, Fu H, Hu L. Efficient Copper-Catalyzed Sonogashira Couplings of Aryl Halides with Terminal Alkynes in Water Synlett. 2011: 702-706. DOI: 10.1055/S-0030-1259542 |
0.426 |
|
| 2010 |
Wang C, Li S, Liu H, Jiang Y, Fu H. Copper-catalyzed synthesis of quinazoline derivatives via Ullmann-type coupling and aerobic oxidation. The Journal of Organic Chemistry. 75: 7936-8. PMID 20964407 DOI: 10.1021/Jo101685D |
0.483 |
|
| 2010 |
Xu H, Li S, Liu H, Fu H, Jiang Y. Simple and efficient copper-catalyzed cascade synthesis of naphthols containing multifunctional groups under mild conditions. Chemical Communications (Cambridge, England). 46: 7617-9. PMID 20848012 DOI: 10.1039/C0Cc01544J |
0.434 |
|
| 2010 |
Gong X, Yang H, Liu H, Jiang Y, Zhao Y, Fu H. Simple and efficient copper-catalyzed approach to 2,4-disubstituted imidazolones. Organic Letters. 12: 3128-31. PMID 20560659 DOI: 10.1021/Ol1008813 |
0.458 |
|
| 2010 |
Lu J, Gong X, Yang H, Fu H. Concise copper-catalyzed one-pot tandem synthesis of benzimidazo[1,2-b]isoquinolin-11-one derivatives. Chemical Communications (Cambridge, England). 46: 4172-4. PMID 20527726 DOI: 10.1039/C0Cc00185F |
0.502 |
|
| 2010 |
Zhao H, Fu H, Qiao R. Copper-catalyzed direct amination of ortho-functionalized haloarenes with sodium azide as the amino source. The Journal of Organic Chemistry. 75: 3311-6. PMID 20359203 DOI: 10.1021/Jo100345T |
0.423 |
|
| 2010 |
Yang D, Fu H. A simple and practical copper-catalyzed approach to substituted phenols from aryl halides by using water as the solvent. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 2366-70. PMID 20108283 DOI: 10.1002/Chem.200903468 |
0.385 |
|
| 2010 |
Fu H, Guo Q, Yang H, Liu H, Jiang Y. Easy and Efficient Copper-Catalyzed Synthesis of Bicyclic Pyrimidinones under Mild Conditions Synlett. 2010: 2611-2616. DOI: 10.1055/S-0030-1258803 |
0.482 |
|
| 2010 |
Li X, Yang D, Jiang Y, Fu H. Efficient copper-catalyzed N-arylations of nitrogen-containing heterocycles and aliphatic amines in water Green Chemistry. 12: 1097. DOI: 10.1039/C002172E |
0.424 |
|
| 2010 |
Lin C, Fu H, Tu G, Zhao Y. Novel and Convenient Approach to Synthesis of AZT/d4T H-phosphonates Chinese Journal of Chemistry. 22: 225-227. DOI: 10.1002/Cjoc.20040220302 |
0.441 |
|
| 2010 |
Miao Z, Fu H, Feng Y, Han B, Tu G, Zhao Y. Studies on Synthesis and Intramolecular Catalyzed Hydrolysis of Thiophosphoramidate Derivatives of Nucleoside Chinese Journal of Chemistry. 20: 1434-1438. DOI: 10.1002/Cjoc.20020201147 |
0.455 |
|
| 2010 |
Miao Z, Fu H, Tu G, Liu H, Bo H, Zhao Y. Synthesis and Novel Properties of Alkyl Thiophosphoramidate Derivatives of Nucleosides Chinese Journal of Chemistry. 20: 492-496. DOI: 10.1002/Cjoc.20020200515 |
0.429 |
|
| 2010 |
Yang X, Fu H, Qiao R, Jiang Y, Zhao Y. A Simple Copper-Catalyzed Cascade Synthesis of 2-Amino-1H-indole-3-carboxylate Derivatives Advanced Synthesis & Catalysis. 352: 1033-1038. DOI: 10.1002/Adsc.200900887 |
0.53 |
|
| 2010 |
Rao H, Fu H, Jiang Y, Zhao Y. Highly Efficient Copper-Catalyzed Synthesis of Internal AlkynesviaAerobic Oxidative Arylation of Terminal Alkynes Advanced Synthesis & Catalysis. 352: 458-462. DOI: 10.1002/Adsc.200900723 |
0.462 |
|
| 2009 |
Yang D, Fu H, Hu L, Jiang Y, Zhao Y. Environmentally friendly iron-catalyzed cascade synthesis of 1,2,4-benzothiadiazine 1,1-dioxide and quinazolinone derivatives. Journal of Combinatorial Chemistry. 11: 653-7. PMID 19505074 DOI: 10.1021/Cc9000339 |
0.45 |
|
| 2009 |
Wang F, Liu H, Fu H, Jiang Y, Zhao Y. An efficient one-pot copper-catalyzed approach to isoquinolin-1(2H)-one derivatives. Organic Letters. 11: 2469-72. PMID 19422263 DOI: 10.1021/Ol900847T |
0.48 |
|
| 2009 |
Rao H, Fu H, Jiang Y, Zhao Y. Easy copper-catalyzed synthesis of primary aromatic amines by couplings aromatic boronic acids with aqueous ammonia at room temperature. Angewandte Chemie (International Ed. in English). 48: 1114-6. PMID 19116995 DOI: 10.1002/Anie.200805424 |
0.451 |
|
| 2009 |
Liu X, Fu H, Jiang Y, Zhao Y. A simple and efficient approach to quinazolinones under mild copper-catalyzed conditions. Angewandte Chemie (International Ed. in English). 48: 348-51. PMID 19053126 DOI: 10.1002/Anie.200804675 |
0.394 |
|
| 2009 |
Fu H, Qiao R, Huang X, Yang H, Zhao Y. Efficient Copper-Catalyzed Synthesis
of 2-Amino-4(3H)-quinazolinone and 2-Aminoquinazoline
Derivatives Synthesis. 2009: 2679-2688. DOI: 10.1055/S-0029-1216871 |
0.52 |
|
| 2009 |
Yang D, Liu H, Yang H, Fu H, Hu L, Jiang Y, Zhao Y. Copper-Catalyzed Synthesis of 1,2,4-Benzothiadiazine 1,1-Dioxide Derivatives by Coupling of 2-Halobenzenesulfonamides with Amidines Advanced Synthesis & Catalysis. 351: 1999-2004. DOI: 10.1002/Adsc.200900101 |
0.483 |
|
| 2009 |
Zeng L, Fu H, Qiao R, Jiang Y, Zhao Y. Efficient Copper-Catalyzed Synthesis ofN-Alkylanthranilic Acidsviaanortho-Substituent Effect of the Carboxyl Group of 2-Halobenzoic Acids at Room Temperature Advanced Synthesis & Catalysis. 351: 1671-1676. DOI: 10.1002/Adsc.200900065 |
0.519 |
|
| 2009 |
Wang F, Liu H, Fu H, Jiang Y, Zhao Y. Highly Efficient Iron(II) Chloride/N-Bromosuccinimide-Mediated Synthesis of Imides and Acylsulfonamides Advanced Synthesis & Catalysis. 351: 246-252. DOI: 10.1002/Adsc.200800668 |
0.405 |
|
| 2008 |
Huang C, Fu Y, Fu H, Jiang Y, Zhao Y. Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives. Chemical Communications (Cambridge, England). 6333-5. PMID 19048146 DOI: 10.1039/B814011A |
0.5 |
|
| 2008 |
Wang L, Fu H, Jiang Y, Zhao Y. Highly efficient copper-catalyzed amidation of aldehydes by C-H activation. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 10722-6. PMID 18855954 DOI: 10.1002/Chem.200801620 |
0.495 |
|
| 2008 |
Yang D, Fu H, Hu L, Jiang Y, Zhao Y. Copper-catalyzed synthesis of benzimidazoles via cascade reactions of o-haloacetanilide derivatives with amidine hydrochlorides. The Journal of Organic Chemistry. 73: 7841-4. PMID 18754576 DOI: 10.1021/Jo8014984 |
0.481 |
|
| 2008 |
Gao X, Fu H, Qiao R, Jiang Y, Zhao Y. Copper-catalyzed synthesis of primary arylamines via cascade reactions of aryl halides with amidine hydrochlorides. The Journal of Organic Chemistry. 73: 6864-6. PMID 18662031 DOI: 10.1021/Jo800818E |
0.487 |
|
| 2008 |
Liu X, Zhang Y, Wang L, Fu H, Jiang Y, Zhao Y. General and efficient copper-catalyzed amidation of saturated C-H bonds using N-halosuccinimides as the oxidants. The Journal of Organic Chemistry. 73: 6207-12. PMID 18593184 DOI: 10.1021/Jo800624M |
0.456 |
|
| 2008 |
Niu M, Yin Z, Fu H, Jiang Y, Zhao Y. Copper-catalyzed coupling of tertiary aliphatic amines with terminal alkynes to propargylamines via C-H activation. The Journal of Organic Chemistry. 73: 3961-3. PMID 18407687 DOI: 10.1021/Jo800279J |
0.436 |
|
| 2008 |
Wang Z, Zhang Y, Fu H, Jiang Y, Zhao Y. Efficient intermolecular iron-catalyzed amidation of C-H bonds in the presence of N-bromosuccinimide. Organic Letters. 10: 1863-6. PMID 18386905 DOI: 10.1021/Ol800593P |
0.404 |
|
| 2008 |
Fu H, Wang Z, Jiang Y, Zhao Y. Iron/Copper-Cocatalyzed
Ullmann N,O-Arylation Using FeCl3, CuO, and rac-1,1′-Binaphthyl-2,2′-diol Synlett. 2008: 2540-2546. DOI: 10.1055/S-2008-1078214 |
0.461 |
|
| 2008 |
Fu H, Niu M, Jiang Y, Zhao Y. A Convenient and Practical Approach to α-Diketones via Reactions of Internal Aryl Alkynes withN-Iodosuccinimide/Water Synthesis. 2008: 2879-2882. DOI: 10.1055/S-2008-1067240 |
0.34 |
|
| 2008 |
Fu H, Qiao R, Jiang Y, Zhao Y, Jiang H. Palladium-Free Copper-Catalyzed Sonogashira Cross-Coupling at Room Temperature Synthesis. 2008: 2417-2426. DOI: 10.1055/S-2008-1067127 |
0.441 |
|
| 2008 |
Fu H, Liu X, Jiang Y, Zhao Y. Highly Efficient Copper-Catalyzed O-Arylation Using Readily Available (S)-N-Methylpyrrolidine-2-Carboxamide as the Ligand Synlett. 2008: 221-224. DOI: 10.1055/S-2007-1000878 |
0.465 |
|
| 2008 |
Fu H, Wang Z, Zhang Y, Jiang Y, Zhao Y. FeCl2-Catalyzed
Aminobromination of Alkenes Using Amides or Sulfonamides
and NBS as the Nitrogen and Bromine Sources Synlett. 2008: 2667-2670. DOI: 10.1055/S-0028-1083509 |
0.411 |
|
| 2008 |
Fu H, Jiang D, Jiang Q, Jiang Y, Zhao Y. Efficient Copper-Catalyzed Coupling
of 2-Haloacetanilides with Phosphine Oxides and Phosphites under
Mild Conditions Synthesis. 2008: 3473-3477. DOI: 10.1055/S-0028-1083155 |
0.473 |
|
| 2008 |
Wang F, Fu H, Jiang Y, Zhao Y. Quick and highly efficient copper-catalyzed cycloaddition of aliphatic and aryl azides with terminal alkynes “on water” Green Chemistry. 10: 452. DOI: 10.1039/B718051A |
0.471 |
|
| 2008 |
Wang F, Fu H, Jiang Y, Zhao Y. Copper-Catalyzed Cycloaddition of Sulfonyl Azides with Alkynes to SynthesizeN-Sulfonyltriazoles ‘on Water’ at Room Temperature Advanced Synthesis & Catalysis. 350: 1830-1834. DOI: 10.1002/Adsc.200800291 |
0.404 |
|
| 2007 |
Zhang Y, Fu H, Jiang Y, Zhao Y. Copper-catalyzed amidation of sp3 C-H bonds adjacent to a nitrogen atom. Organic Letters. 9: 3813-6. PMID 17696547 DOI: 10.1021/Ol701715M |
0.38 |
|
| 2007 |
Jiang D, Fu H, Jiang Y, Zhao Y. CuBr/rac-BINOL-catalyzed N-arylations of aliphatic amines at room temperature. The Journal of Organic Chemistry. 72: 672-4. PMID 17221996 DOI: 10.1021/Jo062060E |
0.415 |
|
| 2007 |
Rao H, Jin Y, Fu H, Jiang Y, Zhao Y. A versatile and efficient ligand for copper-catalyzed formation of C-N, C-O, and P-C bonds: pyrrolidine-2-phosphonic acid phenyl monoester. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 3636-46. PMID 16485315 DOI: 10.1002/Chem.200501473 |
0.442 |
|
| 2007 |
Jiang Q, Jiang D, Jiang Y, Fu H, Zhao Y. A mild and efficient method for copper-catalyzed ullmann-type N-arylation of aliphatic amines and amino acids Synlett. 2007: 1836-1842. DOI: 10.1055/S-2007-982564 |
0.504 |
|
| 2007 |
Fu H, Jin Y, Yin Y, Jiang Y, Zhao Y. Efficient Ring-Closure Approach via Copper-Catalyzed Reactions of Sulfonyl Azide, Terminal Alkynes and Alcohols/Amines Synlett. 2007: 0901-0904. DOI: 10.1055/S-2007-973883 |
0.444 |
|
| 2006 |
Niu M, Fu H, Jiang Y, Zhao Y. Copper-catalyzed addition of H-phosphine oxides to alkynes forming alkenylphosphine oxides. Chemical Communications (Cambridge, England). 272-4. PMID 17299636 DOI: 10.1039/B613416E |
0.422 |
|
| 2006 |
Huang C, Tang X, Fu H, Jiang Y, Zhao Y. Proline/pipecolinic acid-promoted copper-catalyzed P-arylation. The Journal of Organic Chemistry. 71: 5020-2. PMID 16776539 DOI: 10.1021/Jo060492J |
0.444 |
|
| 2006 |
Li X, Wang Y, Fu H, Jiang Y, Zhao Y. Alkylation reactions of phosphachroman-2,4-diones and 4-hydroxy phosphacoumarins. Bioorganic Chemistry. 34: 105-13. PMID 16524614 DOI: 10.1016/J.Bioorg.2006.01.003 |
0.434 |
|
| 2006 |
Zhu J, Fu H, Jiang Y, Zhao Y. A general and chemoselective synthesis of phosphoramidates through reaction of silylated nucleoside di- and triphosphates with silylated amines containing multifunctional groups. The Journal of Organic Chemistry. 71: 1722-4. PMID 16468833 DOI: 10.1021/Jo0521403 |
0.447 |
|
| 2006 |
Rao H, Fu H, Jiang Y, Zhao Y. Copper-catalyzed arylation of amines using diphenyl pyrrolidine-2-phosphonate as the new ligand. The Journal of Organic Chemistry. 70: 8107-9. PMID 16277335 DOI: 10.1021/Jo051221W |
0.431 |
|
| 2006 |
Li X, Zhang D, Pang H, Shen F, Fu H, Jiang Y, Zhao Y. Synthesis of a diverse series of phosphacoumarins with biological activity. Organic Letters. 7: 4919-22. PMID 16235922 DOI: 10.1021/Ol051871M |
0.339 |
|
| 2006 |
Yang T, Lin C, Fu H, Jiang Y, Zhao Y. Copper-catalyzed synthesis of medium- and large-sized nitrogen heterocycles via N-arylation of phosphoramidates and carbamates. Organic Letters. 7: 4781-4. PMID 16209534 DOI: 10.1021/Ol052126C |
0.475 |
|
| 2006 |
Zhu J, Han B, Fu H, Jiang Y, Zhao Y. Novel synthesis of nucleoside 5'-phosphoramidates through reaction of nucleoside triphosphates with amines mediated by trimethylsilyl chloride. The Journal of Organic Chemistry. 70: 6676-9. PMID 16095286 DOI: 10.1021/Jo050716I |
0.39 |
|
| 2006 |
Fu H, Jin Y, Liu J, Yin Y, Jiang Y, Zhao Y. Dimethylaminomethylphosphonic Acid Derivatives-Promoted CuI-Catalyzed Synthesis of Aryl Ethers Synlett. 2006: 1564-1568. DOI: 10.1055/S-2006-941587 |
0.472 |
|
| 2006 |
Li X, Shen F, Fu H, Jiang Y, Zhao Y. Synthesis of 4-Substituted Phosphacoumarins via Cross-Coupling of 4-Tosylphosphacoumarins with Organozinc Reagents Synlett. 2006: 630-632. DOI: 10.1055/S-2006-926245 |
0.393 |
|
| 2006 |
Guo X, Rao H, Fu H, Jiang Y, Zhao Y. An Inexpensive and Efficient Copper Catalyst forN-Arylation of Amines, Amides and Nitrogen-Containing Heterocycles Advanced Synthesis & Catalysis. 348: 2197-2202. DOI: 10.1002/Adsc.200606198 |
0.446 |
|
| 2005 |
Guo X, Jiang P, Fu H, Jiang Y, Zhao Y. New and one pot chemoselective synthesis of nucleoside 5'-H-phosphonate diesters. Nucleosides, Nucleotides & Nucleic Acids. 24: 1325-31. PMID 16252669 DOI: 10.1080/15257770500230467 |
0.334 |
|
| 2005 |
Yang T, Lin C, Fu H, Jiang Y, Zhao Y. Synthesis of sterically hindered peptide analogs using diphenyl phosphite as the coupling reagent. Bioorganic Chemistry. 33: 386-92. PMID 16005935 DOI: 10.1016/J.Bioorg.2005.05.003 |
0.375 |
|
| 2005 |
Lin C, Fu H, Zhao Y, Cheng C. Synthesis of nucleoside N-phosphoamino acids and peptide formation. Origins of Life and Evolution of the Biosphere : the Journal of the International Society For the Study of the Origin of Life. 35: 11-7. PMID 15889647 DOI: 10.1007/S11084-005-0173-X |
0.383 |
|
| 2005 |
Wu YW, Xiao Q, Jiang YY, Fu H, Ju Y, Zhao YF. Synthesis, in vitro anticancer evaluation, and interference with cell cycle progression of N-phosphoamino acid esters of zidovudine and stavudine. Nucleosides, Nucleotides & Nucleic Acids. 23: 1797-811. PMID 15598079 DOI: 10.1081/Ncn-200034057 |
0.301 |
|
| 2005 |
Jiang P, Guo X, Fu H, Jiang Y, Zhao Y. One-Pot Synthesis of Aryl Phosphoramidate Derivatives of AZT/d4T as Anti-HIV Prodrugs Synlett. 2005: 2537-2539. DOI: 10.1055/S-2005-917085 |
0.412 |
|
| 2005 |
Fu H, Zhu J, Jiang Y, Zhao Y. Convenient and Regioselective Synthesis of Nucleoside Phosphoramidate Monoesters Synlett. 2005: 1927-1929. DOI: 10.1055/S-2005-871582 |
0.482 |
|
| 2005 |
Fu H, Tang X, Huang C, Zhao Y. Convenient and Efficient Approach to Di- and Trideoxyribonucleotide N3′→P5′ Phosphoramidates Synlett. 2005: 1930-1932. DOI: 10.1055/S-2005-871580 |
0.437 |
|
| 2004 |
Chen Y, Sun X, Fu H, Liu X, Zhao Y. Novel benzyl rearrangements in electrospray ionization multistage tandem mass spectra of benzyl 2',3'- didehydro-2',3'-dideoxythymidin-5'-yl H-phosphonate. Journal of Mass Spectrometry : Jms. 39: 730-5. PMID 15282751 DOI: 10.1002/Jms.643 |
0.311 |
|
| 2004 |
Li Z, Fu H, Gong H, Zhao Y. Convenient solid-phase synthesis of oligopeptides using pentacoordinated phosphoranes with amino acid residue as building blocks. Bioorganic Chemistry. 32: 170-7. PMID 15110194 DOI: 10.1016/J.Bioorg.2003.12.001 |
0.379 |
|
| 2004 |
Jin Y, Sun M, Fu H, Zhao Y. Synthesis of Novel 5'-Hydrogenphosphonothioate Derivatives of AZT, d4T and ddI Chemistry Letters. 33: 116-117. DOI: 10.1246/Cl.2004.116 |
0.4 |
|
| 2004 |
Yang T, Lin C, Fu H, Jiang Y, Zhao Y. An Efficient Method for Synthesis of 4‐(Phosphonomethyl)benzene Derivatives Under Solvent‐Free Conditions Synthetic Communications. 34: 1017-1022. DOI: 10.1081/Scc-120028632 |
0.475 |
|
| 2004 |
Fu H, Li X, Jiang Y, Zhao Y, Liu J. New and Efficient Approach to Aryl Phosphoramidate Derivatives of AZT/d4T as Anti-HIV Prodrugs Synlett. 2004: 2600-2602. DOI: 10.1055/S-2004-834800 |
0.389 |
|
| 2003 |
Fu H, Han B, Zhao YF, Tu GZ, Xu L, Lu Q, Wang JZ, Xiao HZ. Synthesis and hydrolysis of a phenylalanyl adenylate pentacoordinated phosphorane. Bioorganic Chemistry. 31: 122-8. PMID 12729569 DOI: 10.1016/S0045-2068(03)00023-3 |
0.417 |
|
| 2003 |
Fu H, Han B, Zhao YF. Reaction of ADP with amino acid methyl esters mediated by trimethylsilyl chloride. Chemical Communications (Cambridge, England). 134-5. PMID 12611002 DOI: 10.1039/B207992E |
0.381 |
|
| 2003 |
Lin C, Fu H, Tu G, Zhao Y. Synthesis and Resolution of Dinucleotide(TpAZT) Phosphoramidates Synthetic Communications. 33: 2553-2562. DOI: 10.1081/Scc-120021847 |
0.417 |
|
| 2003 |
Fu H, Xu J, Wang R, Chen Z, Tu G, Wang Q, Zhao Y. Synthesis, Crystal Structure, and Diastereomeric Transfer of Pentacoordinated Phosphoranes Containing Valine or Iso-Leucine Residue Phosphorus Sulfur and Silicon and the Related Elements. 178: 1963-1971. DOI: 10.1080/10426500390228648 |
0.315 |
|
| 2003 |
Lin C, Fu H, Tu G, Zhao Y. Synthesis of Dinucleotide Thiophosphoramidates as Anti-HIV New Prodrugs Synthesis. 2003: 1989-1994. DOI: 10.1055/S-2003-41039 |
0.371 |
|
| 2003 |
Miao Z, Fu H, Tu G, Zhu J, Ai H, Zhao Y. A Stepwise one‐pot synthesis of aryl N‐phosphonamidothionate derivatives of nucleosides Heteroatom Chemistry. 14: 62-66. DOI: 10.1002/Hc.10080 |
0.39 |
|
| 2002 |
Chen J, Chen Y, Niu YL, Fu H, Zhao YF. A carbonyl oxygen migration in electrospray ionization mass spectrometry and its application in differentiating alpha- and beta-alanyl peptides. Journal of Mass Spectrometry : Jms. 37: 934-9. PMID 12271436 DOI: 10.1002/Jms.352 |
0.313 |
|
| 2002 |
Miao Z, Fu H, Tu G, Zhao Y. ONE POT SYNTHESIS OF ARYL THIOPHOSPHORAMIDATE DERIVATIVES OF AZT Synthetic Communications. 32: 3301-3309. DOI: 10.1081/Scc-120014036 |
0.366 |
|
| 2002 |
Miao Z, Fu H, Han B, Chen Y, Zhao Y. A STEPWISE ONE POT SYNTHESIS OF ALKYL THIOPHOSPHORAMIDATE DERIVATIVES OF NUCLEOSIDES Synthetic Communications. 32: 1159-1167. DOI: 10.1081/Scc-120003605 |
0.402 |
|
| 2002 |
Miao Z, Fu H, Han B, Zhao Y. ONE POT SYNTHESIS OF NUCLEOSIDE 5′-THIOPHOSPHORAMIDATES Synthetic Communications. 32: 1069-1076. DOI: 10.1081/Scc-120003155 |
0.406 |
|
| 2002 |
Miao Z, Fu H, Han B, Zhao Y. Synthesis of N -Phosphonamidothionate Derivatives of Nucleoside Phosphorus, Sulfur, and Silicon and the Related Elements. 177: 2089-2090. DOI: 10.1080/10426500213449 |
0.405 |
|
| 2002 |
Miao Z, Fu H, Han B, Chen Y, Zhao Y. A Convenient Two-Step One-Pot Synthesis of Alkylthiophosphoramidates Derivatives Phosphorus, Sulfur, and Silicon and the Related Elements. 177: 641-646. DOI: 10.1080/10426500210257 |
0.439 |
|
| 2001 |
Dong S, Fu H, Zhao Y. SYNTHESIS OF N-PHOSPHOPEPTIDES COUPLED BY DICHLOROTRIPHENYLPHOSPHORANE Synthetic Communications. 31: 2067-2075. DOI: 10.1081/Scc-100104428 |
0.419 |
|
| 2000 |
Jiang Y, Fu H, Xu L, Lu Q, Wang J, Zhao Y. Identification of self‐assembly products from N‐phosphoamino acids by electrospray ionization mass spectrometry Rapid Communications in Mass Spectrometry. 14: 1491-1493. PMID 10931543 DOI: 10.1002/1097-0231(20000830)14:16<1491::Aid-Rcm54>3.0.Co;2-0 |
0.309 |
|
| 2000 |
Zhao Y, Han B, Zhao G, Fu H. Synthesis of Novel Nα, Nγ-Lysine Linked Dinucleotides Synthetic Communications. 30: 3141-3151. DOI: 10.1080/00397910008086923 |
0.385 |
|
| 1999 |
Li Z, Fu H, Gong H, Zhao Y. 31P NMR Spectral Evidence for the Hexacoordinated Phosphorus Intermediates in the Reaction of Oxyphosphorochloridate With Amino Acids Phosphorus, Sulfur, and Silicon and the Related Elements. 147: 215-215. DOI: 10.1080/10426509908053588 |
0.353 |
|
| 1999 |
Fu H, Li Z, Zhao Y, Tu G. Oligomerization ofN,O-Bis(trimethylsilyl)-α-amino Acids into Peptides Mediated byo-Phenylene Phosphorochloridate Journal of the American Chemical Society. 121: 291-295. DOI: 10.1021/Ja980662C |
0.313 |
|
| 1998 |
Fu H, LI X, Li Z, Wang J, Zhao Y. Studies on the Mechanism of Some Bioorganic Reactions for N-Phosphoamino Acids Phosphorus, Sulfur, and Silicon and the Related Elements. 134: 177-186. DOI: 10.1080/10426509808545461 |
0.414 |
|
| 1998 |
Lu H, Zhang N, Chen X, Fu H, Zhao Y. Direct Thiophosphorylation Of Amino Acids And Peptides Synthetic Communications. 28: 1727-1736. DOI: 10.1080/00397919808007003 |
0.327 |
|
| 1998 |
Fu H, Tu G, Li Z, Zhao Y. Synthesis of 2-Phenoxy-2,75-spiro[1,3,2-benzodioxaphosphole-2,2′-1,3,2-oxazophospholan]-5′-ones Synthesis. 1998: 855-858. DOI: 10.1055/S-1998-2086 |
0.375 |
|
| 1998 |
Fu H, Li Z, Zhao Y, Xiao H, Wang J. Self-assembly of N,O-bis(trimethylsilyl)amino acids to peptides mediated byo-phenylene phosphorochloridate identified by fast atom bombardment mass spectrometry Rapid Communications in Mass Spectrometry. 12: 94-96. DOI: 10.1002/(Sici)1097-0231(19980131)12:2<94::Aid-Rcm114>3.0.Co;2-7 |
0.301 |
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