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For: Slagbrand T, Kervefors G, Tinnis F, Adolfsson H. An Efficient One-pot Procedure for the Direct Preparation of 4,5-Dihydroisoxazoles from Amides. Adv Synth Catal 2017;359:1990-5. [DOI: 10.1002/adsc.201700154] [Cited by in Crossref: 24] [Cited by in F6Publishing: 29] [Article Influence: 4.8] [Reference Citation Analysis]
Number Citing Articles
1 Luo K, Zhao Y, Tang Z, Li W, Lin J, Jin Y. Visible-Light-Induced Dual C(sp3)-H Bond Functionalization of Tertiary Amine via Hydrogen Transfer to Carbene and Subsequent Cycloaddition. Org Lett 2022. [PMID: 35985018 DOI: 10.1021/acs.orglett.2c02557] [Reference Citation Analysis]
2 Wu DP, Ou W, Huang PQ. Ir-Catalyzed Chemoselective Reductive Condensation Reactions of Tertiary Amides with Active Methylene Compounds. Org Lett 2022. [PMID: 35849542 DOI: 10.1021/acs.orglett.2c02045] [Reference Citation Analysis]
3 Zhang L, Wang R, Wang C, Liu B, Yang J, Zhang Z, Huang J, Yang Z. Concise Synthesis of 7-Deoxypsammaplysins K and O and 7-Deoxyceratinamide A by 1,3-Dipole Cycloaddition. Org Lett . [DOI: 10.1021/acs.orglett.2c01298] [Reference Citation Analysis]
4 Agrawal T, Perez-Morales KD, Cort JA, Sieber JD. Asymmetric Synthesis of Propargylic α-Stereogenic Tertiary Amines by Reductive Alkynylation of Tertiary Amides Using Ir/Cu Tandem Catalysis. J Org Chem 2022. [PMID: 35435681 DOI: 10.1021/acs.joc.2c00131] [Reference Citation Analysis]
5 Li Z, Zhao F, Ou W, Huang P, Wang X. Asymmetric Deoxygenative Alkynylation of Tertiary Amides Enabled by Iridium/Copper Bimetallic Relay Catalysis. Angew Chem 2021;133:26808-13. [DOI: 10.1002/ange.202111029] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
6 Li Z, Zhao F, Ou W, Huang PQ, Wang X. Asymmetric Deoxygenative Alkynylation of Tertiary Amides Enabled by Iridium/Copper Bimetallic Relay Catalysis. Angew Chem Int Ed Engl 2021. [PMID: 34596947 DOI: 10.1002/anie.202111029] [Cited by in F6Publishing: 9] [Reference Citation Analysis]
7 Matheau-Raven D, Dixon DJ. General α-Amino 1,3,4-Oxadiazole Synthesis via Late-Stage Reductive Functionalization of Tertiary Amides and Lactams*. Angew Chem Int Ed Engl 2021;60:19725-9. [PMID: 34191400 DOI: 10.1002/anie.202107536] [Cited by in F6Publishing: 9] [Reference Citation Analysis]
8 Matheau‐raven D, Dixon DJ. General α‐Amino 1,3,4‐Oxadiazole Synthesis via Late‐Stage Reductive Functionalization of Tertiary Amides and Lactams**. Angew Chem 2021;133:19877-81. [DOI: 10.1002/ange.202107536] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 Yan F, Huang Z, Du C, Bai J, Li Y. Iron-catalyzed reductive strecker reaction. Journal of Catalysis 2021;395:188-94. [DOI: 10.1016/j.jcat.2021.01.003] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
10 Lugovik KI, Kanaa A, Benassi E, Belskaya NP. Fluorescent Assembles of 2‐Amino‐3‐cyanothiophenes with Azoles. Design and Peculiar Properties of Absorption and Emission. Asian J Org Chem 2021;10:400-11. [DOI: 10.1002/ajoc.202000663] [Reference Citation Analysis]
11 Rogova T, Gabriel P, Zavitsanou S, Leitch JA, Duarte F, Dixon DJ. Reverse Polarity Reductive Functionalization of Tertiary Amides via a Dual Iridium-Catalyzed Hydrosilylation and Single Electron Transfer Strategy. ACS Catal 2020;10:11438-47. [DOI: 10.1021/acscatal.0c03089] [Cited by in Crossref: 20] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
12 Lenshmidt LV, Ledovskaya MS, Larina AG, Filatov AS, Chakchir OB, Uspenskii AA, Stepakov AV. Synthesis of Isoxazolo[5',4':3,4]pyrrolo[1,2-a]azepines via N-Acyliminium Cyclization. Russ J Org Chem 2020;56:234-45. [DOI: 10.1134/s1070428020020098] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Ou W, Huang P. Amides as surrogates of aldehydes for C-C bond formation: amide-based direct Knoevenagel-type condensation reaction and related reactions. Sci China Chem 2020;63:11-5. [DOI: 10.1007/s11426-019-9586-3] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
14 Takahashi Y, Sato T, Chida N. Iridium-catalyzed Reductive Nucleophilic Addition to Tertiary Amides. Chem Lett 2019;48:1138-41. [DOI: 10.1246/cl.190467] [Cited by in Crossref: 16] [Cited by in F6Publishing: 21] [Article Influence: 5.3] [Reference Citation Analysis]
15 Chen H, Huang YH, Ye JL, Huang PQ. Double Addition of Alkynyllithium Reagents to Amides/Lactams: A Direct and Flexible Synthesis of 3-Amino-1,4-diynes Bearing an Aza-Quaternary Carbon Center. J Org Chem 2019;84:9270-81. [PMID: 31287315 DOI: 10.1021/acs.joc.9b01416] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
16 Trillo P, Adolfsson H. Direct Catalytic Reductive N-Alkylation of Amines with Carboxylic Acids: Chemoselective Enamine Formation and further Functionalizations. ACS Catal 2019;9:7588-95. [DOI: 10.1021/acscatal.9b01974] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 4.7] [Reference Citation Analysis]
17 Yi F, Sun Q, Sun J, Fu C, Yi W. Terminal Alkyne-Assisted One-Pot Synthesis of Arylamidines: Carbon Source of the Amidine Group from Oxime Chlorides. J Org Chem 2019;84:6780-7. [PMID: 31074281 DOI: 10.1021/acs.joc.9b00538] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Huang Y, Wang S, Wu D, Huang P. Intermolecular Dehydrative [4 + 2] Aza-Annulation of N -Arylamides with Alkenes: A Direct and Divergent Entrance to Aza-Heterocycles. Org Lett 2019;21:1681-5. [DOI: 10.1021/acs.orglett.9b00233] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 4.3] [Reference Citation Analysis]
19 Trillo P, Slagbrand T, Adolfsson H. Straightforward α-Amino Nitrile Synthesis Through Mo(CO) 6 -Catalyzed Reductive Functionalization of Carboxamides. Angew Chem 2018;130:12527-31. [DOI: 10.1002/ange.201807735] [Cited by in Crossref: 9] [Cited by in F6Publishing: 12] [Article Influence: 2.3] [Reference Citation Analysis]
20 Trillo P, Slagbrand T, Adolfsson H. Straightforward α-Amino Nitrile Synthesis Through Mo(CO) 6 -Catalyzed Reductive Functionalization of Carboxamides. Angew Chem Int Ed 2018;57:12347-51. [DOI: 10.1002/anie.201807735] [Cited by in Crossref: 28] [Cited by in F6Publishing: 37] [Article Influence: 7.0] [Reference Citation Analysis]
21 Ou W, Han F, Hu X, Chen H, Huang P. Iridium-Catalyzed Reductive Alkylations of Secondary Amides. Angew Chem 2018;130:11524-8. [DOI: 10.1002/ange.201806747] [Cited by in Crossref: 16] [Cited by in F6Publishing: 22] [Article Influence: 4.0] [Reference Citation Analysis]
22 Ou W, Han F, Hu X, Chen H, Huang P. Iridium-Catalyzed Reductive Alkylations of Secondary Amides. Angew Chem Int Ed 2018;57:11354-8. [DOI: 10.1002/anie.201806747] [Cited by in Crossref: 34] [Cited by in F6Publishing: 48] [Article Influence: 8.5] [Reference Citation Analysis]
23 Yang ZP, He Q, Ye JL, Huang PQ. Asymmetric Total Synthesis and Absolute Configuration Determination of (-)-Verrupyrroloindoline. Org Lett 2018;20:4200-3. [PMID: 29969900 DOI: 10.1021/acs.orglett.8b01579] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]
24 Hu X, Shen T, Cai D, Zheng J, Huang P. The iridium-catalysed reductive coupling reaction of tertiary lactams/amides with isocyanoacetates. Org Chem Front 2018;5:2051-6. [DOI: 10.1039/c8qo00312b] [Cited by in Crossref: 19] [Article Influence: 4.8] [Reference Citation Analysis]
25 Chen H, Ye J, Huang P. Chemoselective direct reductive trifluoromethylation of amides: a flexible access to functionalized α-trifluoromethylamines. Org Chem Front 2018;5:943-7. [DOI: 10.1039/c7qo01031a] [Cited by in Crossref: 16] [Article Influence: 4.0] [Reference Citation Analysis]
26 Sato T, Yoritate M, Tajima H, Chida N. Total synthesis of complex alkaloids by nucleophilic addition to amides. Org Biomol Chem 2018;16:3864-75. [DOI: 10.1039/c8ob00733k] [Cited by in Crossref: 49] [Cited by in F6Publishing: 4] [Article Influence: 12.3] [Reference Citation Analysis]
27 Yoritate M, Takahashi Y, Tajima H, Ogihara C, Yokoyama T, Soda Y, Oishi T, Sato T, Chida N. Unified Total Synthesis of Stemoamide-Type Alkaloids by Chemoselective Assembly of Five-Membered Building Blocks. J Am Chem Soc 2017;139:18386-91. [PMID: 29179540 DOI: 10.1021/jacs.7b10944] [Cited by in Crossref: 56] [Cited by in F6Publishing: 44] [Article Influence: 11.2] [Reference Citation Analysis]
28 Huang P, Fan T. Intramolecular Keto Lactam Condensation: A Convenient and Straightforward Approach to Bicyclic Vinylogous Lactams: Intramolecular Keto Lactam Condensation: A Convenient and Straightforward Approach to Bicyclic Vinylogous Lactams. Eur J Org Chem 2017;2017:6369-74. [DOI: 10.1002/ejoc.201701060] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 2.4] [Reference Citation Analysis]
29 Huang P, Chen H. Ni-Catalyzed cross-coupling reactions of N -acylpyrrole-type amides with organoboron reagents. Chem Commun 2017;53:12584-7. [DOI: 10.1039/c7cc07457c] [Cited by in Crossref: 41] [Cited by in F6Publishing: 5] [Article Influence: 8.2] [Reference Citation Analysis]