Year |
Citation |
Score |
2020 |
Devi R, Mukhopadhyay S, Jyoti Das A, Kumar Das S. Base-mediated synthesis of benzimidazole-fused 1,4-benzoxazepines via sequential intermolecular epoxide ring-opening/intramolecular SNAr reactions Tetrahedron Letters. 61: 152491. DOI: 10.1016/J.TETLET.2020.152491 |
0.426 |
|
2018 |
Devi R, Das J, Sarma B, Das SK. Phenolate-induced intramolecular ring-opening cyclization of N-tosylaziridines: access to functionalized benzoxacycles. Organic & Biomolecular Chemistry. PMID 30070284 DOI: 10.1039/c8ob01143e |
0.561 |
|
2018 |
Devi R, Das SK. Combining spiro-fused cyclohexadienone – tetrahydrofuran ring system with glycine: Asymmetric synthesis of a new class of α-amino acid derivatives Tetrahedron Letters. 59: 2281-2283. DOI: 10.1016/J.TETLET.2018.04.084 |
0.355 |
|
2017 |
Devi R, Das SK. Studies directed toward the exploitation of vicinal diols in the synthesis of (+)-nebivolol intermediates. Beilstein Journal of Organic Chemistry. 13: 571-578. PMID 28405237 DOI: 10.3762/bjoc.13.56 |
0.484 |
|
2017 |
Borgohain H, Devi R, Dheer D, Borah BJ, Shankar R, Das SK. Synthesis of Tetrahydroquinoline-Embedded Bridged Benzothiaoxazepine-1,1-dioxides European Journal of Organic Chemistry. 2017: 6671-6679. DOI: 10.1002/EJOC.201701152 |
0.442 |
|
2016 |
Gogoi D, Devi R, Pahari P, Sarma B, Das SK. cis-Diastereoselective synthesis of chroman-fused tetralins as B-ring-modified analogues of brazilin. Beilstein Journal of Organic Chemistry. 12: 2816-2822. PMID 28144354 DOI: 10.3762/bjoc.12.280 |
0.513 |
|
2016 |
Devi R, Gogoi D, Bora P, Das SK. Synthesis of diverse catechin congeners via diastereoselective intramolecular epoxy-arene cyclization Tetrahedron. 72: 4878-4888. DOI: 10.1016/j.tet.2016.06.059 |
0.407 |
|
2016 |
Devi R, Gogoi D, Bora P, Das SK. ChemInform Abstract: Synthesis of Diverse Catechin Congeners via Diastereoselective Intramolecular Epoxy-Arene Cyclization. Cheminform. 47. DOI: 10.1002/CHIN.201647160 |
0.525 |
|
2015 |
Devi R, Kalita T, Das SK. Brønsted acid-catalysed intramolecular ring opening of 2-(aryloxymethyl)-3-aryloxiranes leading to trans-4-arylchroman-3-ols: scope and limitations Rsc Advances. 5: 39692-39696. DOI: 10.1039/C5RA02193F |
0.344 |
|
2015 |
Devi R, Kalita T, Das SK. ChemInform Abstract: Broensted Acid-Catalyzed Intramolecular Ring Opening of 2-(Aryloxymethyl)-3-aryloxiranes Leading to trans-4-Arylchroman-3-ols: Scope and Limitations. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201537168 |
0.329 |
|
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