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For: Verma AK, Patel M, Joshi M, Likhar PR, Tiwari RK, Parang K. Base-Mediated Chemo- and Stereoselective Addition of 5-Aminoindole/Tryptamine and Histamines onto Alkynes. J Org Chem 2014;79:172-86. [DOI: 10.1021/jo402352v] [Cited by in Crossref: 27] [Cited by in F6Publishing: 17] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Gvozdev VD, Shavrin KN, Baskir EG, Egorov MP, Nefedov OM. Cyclization of alk-4-ynals with o-diaminoarenes as a selective one-pot synthesis of arylmethylidene-substituted 2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazoles and 7,8-dihydro-6H-pyrrolo[1’,2’:1,2]imidazo[4,5-b]pyridines. Russ Chem Bull 2016;65:1829-38. [DOI: 10.1007/s11172-016-1517-6] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
2 Mahdavi M, Hariri R, Saeedi M, Foroumadi A, Shafiee A, Akbarzadeh T. Synthesis of new benzo[f]imidazo[1,2-d][1,4]oxazepines: AgNO3-mediated intramolecular hydroamination. Tetrahedron Letters 2015;56:7082-4. [DOI: 10.1016/j.tetlet.2015.11.014] [Cited by in Crossref: 15] [Cited by in F6Publishing: 5] [Article Influence: 2.1] [Reference Citation Analysis]
3 Mekky AEM, Sanad SMH. Synthesis, Characterization, and Antimicrobial Evaluation of Novel Thiohydrazonates and Pyrazolo[3,4- b ]pyridines. Polycyclic Aromatic Compounds 2021;41:936-49. [DOI: 10.1080/10406638.2019.1631194] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 2.3] [Reference Citation Analysis]
4 Jha RR, Danodia AK, Verma AK. Synthesis of fused heterocycles via preferential hydroamination of o-haloarylalkynes over N-arylation and successive intramolecular CC bond formation. Tetrahedron Letters 2014;55:4724-30. [DOI: 10.1016/j.tetlet.2014.06.092] [Cited by in Crossref: 10] [Article Influence: 1.3] [Reference Citation Analysis]
5 Patel M, Saunthwal RK, Dhaked DK, Bharatam PV, Verma AK. Metal-free Intermolecular Hydrophenoxylation of Aryl Alkynes. Asian J Org Chem 2016;5:213-21. [DOI: 10.1002/ajoc.201500479] [Cited by in Crossref: 9] [Article Influence: 1.3] [Reference Citation Analysis]
6 Patel M, Sushmita, Verma AK. Copper-catalyzed stereo- and chemoselective synthesis of enaminones via Michael type addition. J Chem Sci 2018;130. [DOI: 10.1007/s12039-018-1465-9] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
7 Li Z, Liang Y, Zhu Y, Tan H, Li X, Wang W, Zhang Z, Jiao N. Prroles and Their Benzo Derivatives: Reactivity. Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier; 2020. [DOI: 10.1016/b978-0-12-409547-2.14853-x] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
8 Zhou M, Tan X, Hu Y, Shen HC, Qian X. Highly Chemo- and Regioselective Vinylation of N-Heteroarenes with Vinylsulfonium Salts. J Org Chem 2018;83:8627-35. [PMID: 29799743 DOI: 10.1021/acs.joc.8b00682] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
9 Tantak MP, Malik M, Klingler L, Olson Z, Kumar A, Sadana R, Kumar D. Indolyl-α-keto-1,3,4-oxadiazoles: Synthesis, anti-cell proliferation activity, and inhibition of tubulin polymerization. Bioorg Med Chem Lett 2021;37:127842. [PMID: 33556575 DOI: 10.1016/j.bmcl.2021.127842] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
10 Garg V, Kumar P, Verma AK. Chemo-, Regio-, and Stereoselective N-Alkenylation of Pyrazoles/Benzpyrazoles Using Activated and Unactivated Alkynes. J Org Chem 2017;82:10247-62. [PMID: 28861995 DOI: 10.1021/acs.joc.7b01746] [Cited by in Crossref: 12] [Cited by in F6Publishing: 5] [Article Influence: 2.4] [Reference Citation Analysis]
11 Saunthwal RK, Patel M, Verma AK. Regioselective Synthesis of C-3-Functionalized Quinolines via Hetero-Diels–Alder Cycloaddition of Azadienes with Terminal Alkynes. J Org Chem 2016;81:6563-72. [DOI: 10.1021/acs.joc.6b01186] [Cited by in Crossref: 38] [Cited by in F6Publishing: 26] [Article Influence: 6.3] [Reference Citation Analysis]
12 Ranjan A, Yerande R, Wakchaure PB, Yerande SG, Dethe DH. Base-Mediated Hydroamination of Propargylamine: A Regioselective Intramolecular 5- exo-dig Cycloisomerization en Route to Imidazole-2-thione. Org Lett 2014;16:5788-91. [DOI: 10.1021/ol502871r] [Cited by in Crossref: 56] [Cited by in F6Publishing: 36] [Article Influence: 7.0] [Reference Citation Analysis]
13 Hentz A, Retailleau P, Gandon V, Cariou K, Dodd RH. Transition-Metal-Free Tunable Chemoselective N Functionalization of Indoles with Ynamides. Angew Chem Int Ed 2014;53:8333-7. [DOI: 10.1002/anie.201402767] [Cited by in Crossref: 38] [Cited by in F6Publishing: 26] [Article Influence: 4.8] [Reference Citation Analysis]
14 Csenki JT, Mészáros Á, Gonda Z, Novák Z. Stereoselective Direct N-Trifluoropropenylation of Heterocycles with a Hypervalent Iodonium Reagent. Chemistry 2021;27:15638-43. [PMID: 34549840 DOI: 10.1002/chem.202102840] [Reference Citation Analysis]
15 Hentz A, Retailleau P, Gandon V, Cariou K, Dodd RH. Transition-Metal-Free Tunable Chemoselective N Functionalization of Indoles with Ynamides. Angew Chem 2014;126:8473-7. [DOI: 10.1002/ange.201402767] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 1.8] [Reference Citation Analysis]
16 Patel M, Saunthwal RK, Dhaked DK, Bharatam PV, Verma AK. Nucleophilic Addition versus S N Ar Study: Chemo-, Regio- and Stereoselective Hydrothiolation of Haloaryl Alkynes over S-Arylation of Aryl Halides. Asian J Org Chem 2015;4:894-8. [DOI: 10.1002/ajoc.201500239] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
17 Nie X, Han X, Sun J, Si C, Wei B, Lin G. Nickel-Catalyzed Regioselective Hydroamination of Ynamides with Secondary Amines. J Org Chem 2021;86:3433-43. [DOI: 10.1021/acs.joc.0c02807] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
18 Yang R, Yue S, Tan W, Xie Y, Cai H. DMSO/t-BuONa/O2-Mediated Aerobic Dehydrogenation of Saturated N-Heterocycles. J Org Chem 2020;85:7501-9. [PMID: 32368910 DOI: 10.1021/acs.joc.9b03447] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
19 Morimoto Y, Kochi T, Kakiuchi F. Rhodium-Catalyzed Anti-Markovnikov Hydroamination of Aliphatic and Aromatic Terminal Alkynes with Aliphatic Primary Amines. J Org Chem 2021;86:13143-52. [PMID: 34492192 DOI: 10.1021/acs.joc.1c01636] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Saunthwal RK, Patel M, Verma AK. Metal- and Protection-Free [4 + 2] Cycloadditions of Alkynes with Azadienes: Assembly of Functionalized Quinolines. Org Lett 2016;18:2200-3. [PMID: 27119774 DOI: 10.1021/acs.orglett.6b00817] [Cited by in Crossref: 43] [Cited by in F6Publishing: 28] [Article Influence: 7.2] [Reference Citation Analysis]
21 Gvozdev VD, Shavrin KN, Egorov MP, Nefedov OM. Stereoselective one-pot synthesis of (1Z)- and (1E)-1-arylmethylidene-2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazoles by cyclization of alk-4-ynals with o-diaminobenzene. Mendeleev Communications 2016;26:3-5. [DOI: 10.1016/j.mencom.2016.01.002] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
22 Liu W, Zeng R, Han Y, Wang Y, Tao H, Chen Y, Liu F, Liang Y. Computational and experimental investigation on the BCl 3 promoted intramolecular amination of alkenes and alkynes. Org Biomol Chem 2019;17:2776-83. [DOI: 10.1039/c9ob00264b] [Cited by in Crossref: 7] [Article Influence: 2.3] [Reference Citation Analysis]
23 Patel M, Saunthwal RK, Verma AK. Base-Mediated Hydroamination of Alkynes. Acc Chem Res 2017;50:240-54. [DOI: 10.1021/acs.accounts.6b00449] [Cited by in Crossref: 107] [Cited by in F6Publishing: 61] [Article Influence: 21.4] [Reference Citation Analysis]
24 Liu L, Lei Z, Wang H, Bian M, Liu Z, Liu J, Hu X. Inorganic base-mediated stereoselective hydroamination of arylalkynes with imidazole: An efficient access to N -vinylimidazoles. Tetrahedron 2018;74:4515-20. [DOI: 10.1016/j.tet.2018.07.022] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]