Year |
Citation |
Score |
2023 |
Beng TK, Garcia J, Eichwald J, Borg C. Introducing a sulfone-embedded anhydride to the anhydride-imine reaction for the modular synthesis of N-heterocyclic sulfones bearing vicinal stereocenters. Rsc Advances. 13: 14355-14360. PMID 37180005 DOI: 10.1039/d3ra01812a |
0.337 |
|
2020 |
Moreno A, Beng TK. Direct access to vicinally functionalized and N-trifluoroacetylated (bicyclic)ketopiperazines using a readily affordable N-heterocyclic anhydride. Organic & Biomolecular Chemistry. PMID 32039416 DOI: 10.1039/D0Ob00049C |
0.425 |
|
2020 |
Farah AO, Rabah M, Beng TK. Transition metal-free domino acyl substitution/Michael addition of alkenyl Grignard reagents to lactam esters: synthesis of lactam-bearing homoallylic ketones Rsc Advances. 10: 22454-22459. DOI: 10.1039/D0Ra03885G |
0.373 |
|
2020 |
Beng TK, Garcia J, Smith M, Orellana AO. Skeletal remodelling of α-substituted cyclic eneformamides to α-ketonyl cyclic amines New Journal of Chemistry. 44: 15337-15340. DOI: 10.1039/D0Nj02768E |
0.381 |
|
2020 |
Beng TK, Moreno A. Copper-catalyzed alkenylation of novel N-iodoarylated allylic ketopiperazinonates with unactivated alkenes New Journal of Chemistry. 44: 4257-4261. DOI: 10.1039/C9Nj06178A |
0.489 |
|
2020 |
Beng TK, Omar Farah A. Modular access to formamide-tethered α-halo ynones via the deconstructive oxo-halogenation of readily available α-alkynyl eneformamides Tetrahedron Letters. 61: 151821. DOI: 10.1016/J.Tetlet.2020.151821 |
0.333 |
|
2019 |
Beng TK, Wanjiku F. Iridium-catalyzed α-alkynylation of cyclic nonaromatic eneformamides: application to the synthesis of azapolycyclic architectures New Journal of Chemistry. 43: 4664-4668. DOI: 10.1039/C9Nj00003H |
0.41 |
|
2019 |
Beng TK, Langevin S, Farah AO, Goodsell J, Wyatt K. One-shot access to isoquinolone and (hetero)izidinone architectures using cyclic α-chloro eneformamides and cyclic anhydrides New Journal of Chemistry. 43: 5282-5286. DOI: 10.1039/C8Nj06539J |
0.328 |
|
2018 |
Beng TK, Bauder M, Rodriguez MJ, Moreno A. Copper-catalyzed regioselective dehydrogenative alkoxylation of morpholinonyl alkenols: application to the synthesis of spirotricyclic dihydropyrans and of trans-fused bicyclic morpholines New Journal of Chemistry. 42: 16451-16455. DOI: 10.1039/C8Nj03890B |
0.321 |
|
2018 |
Farah AO, Archibald R, Rodriguez MJ, Moreno A, Dondji B, Beng TK. Flexible access to 2,3,5,6-tetrasubstituted dehydropiperidines by Ni- or Co-catalyzed site-selective cross-coupling using Vilsmeier-Haack-derived α-chloro-β-formyltetrahydropyridines Tetrahedron Letters. 59: 3495-3498. DOI: 10.1016/J.Tetlet.2018.08.023 |
0.385 |
|
2016 |
Braunstein H, Langevin S, Khim M, Adamson J, Hovenkotter K, Kotlarz L, Mansker B, Beng TK. Modular access to vicinally functionalized allylic (thio)morpholinonates and piperidinonates by substrate-controlled annulation of 1,3-azadienes with hexacyclic anhydrides. Organic & Biomolecular Chemistry. 14: 8864-8872. PMID 27714224 DOI: 10.1039/C6Ob01526C |
0.346 |
|
2016 |
Beng TK, Langevin S, Braunstein H, Khim M. Regiocontrolled synthesis of (hetero)aryl and alkenyl dehydropyrrolidines, dehydropiperidines and azepenes by Ru-catalyzed, heteroatom-directed α-C-H activation/cross-coupling of cyclic enamides with boronic acids. Organic & Biomolecular Chemistry. 14: 830-4. PMID 26612230 DOI: 10.1039/C5Ob02263K |
0.348 |
|
2015 |
Beng TK, Fox N, Bassler DP, Alwali A, Sincavage K, Silaire AW. Trapping of carbolithiation-derived tertiary benzylic α-lithio piperidines with carbon electrophiles: Controlling the formation of α-amino quaternary and vicinal stereocenters. Organic & Biomolecular Chemistry. 13: 8647-51. PMID 26205365 DOI: 10.1039/C5Ob01371B |
0.329 |
|
2015 |
Beng TK, Silaire AW, Alwali A, Bassler DP. One-shot access to α,β-difunctionalized azepenes and dehydropiperidines by reductive cross-coupling of α-selenonyl-β-selenyl enamides with organic bromides. Organic & Biomolecular Chemistry. 13: 7915-9. PMID 26135053 DOI: 10.1039/C5Ob01003A |
0.325 |
|
2015 |
Beng TK, Sincavage K, Silaire AW, Alwali A, Bassler DP, Spence LE, Beale O. Direct access to functionalized benzotropones, azepanes, and piperidines by reductive cross-coupling of α-bromo enones with α-bromo enamides. Organic & Biomolecular Chemistry. 13: 5349-53. PMID 25872155 DOI: 10.1039/C5Ob00517E |
0.359 |
|
2015 |
Beng TK, Takeuchi H, Weber M, Sarpong R. Stereocontrolled synthesis of vicinally functionalized piperidines by nucleophilic β-addition of alkyllithiums to α-aryl substituted piperidine enecarbamates. Chemical Communications (Cambridge, England). 51: 7653-6. PMID 25845938 DOI: 10.1039/C5Cc01307K |
0.394 |
|
2015 |
Bassler DP, Spence L, Alwali A, Beale O, Beng TK. Expedient access to α,β-difunctionalized azepenes using α-halo eneformamides: application to the one-pot synthesis of 2-benzazepanes. Organic & Biomolecular Chemistry. 13: 2285-92. PMID 25553911 DOI: 10.1039/C4Ob02183E |
0.355 |
|
2015 |
Beng TK, Fox N. Diastereoselective synthesis of α,α,α′-trisubstituted pyrrolidines and piperidines by directed sequential lithiation/alkylation Dedicated to the memory of Professor Bob Gawley who passed on in March 2013. His mentorship forever will be appreciated Tetrahedron Letters. 56: 119-122. DOI: 10.1016/J.Tetlet.2014.11.031 |
0.342 |
|
2015 |
Bassler DP, Alwali A, Spence L, Beale O, Beng TK. Cobalt-catalyzed arylation and alkenylation of alpha-bromo eneformamides and enecarbamates by cross-coupling with organic bromides: Application to the synthesis of functionalized piperidines and azepanes Journal of Organometallic Chemistry. 780: 6-12. DOI: 10.1016/J.Jorganchem.2015.01.001 |
0.373 |
|
2014 |
Beng TK, Wilkerson-Hill SM, Sarpong R. Direct access to functionalized azepanes by cross-coupling with α-halo eneformamides Organic Letters. 16: 916-919. PMID 24456197 DOI: 10.1021/Ol403671S |
0.343 |
|
2014 |
Beng TK, Wilkerson-Hill SM, Sarpong R. Correction to Direct Access to Functionalized Azepanes by Cross-Coupling with α-Halo Eneformamides Organic Letters. 16: 3170-3170. DOI: 10.1021/Ol5012696 |
0.315 |
|
2014 |
Beng TK, Bassler DP. Vicinal difunctionalization of dehydropiperidines using α-chloro-β-sulfonyl eneformamides Tetrahedron Letters. 55: 6662-6664. DOI: 10.1016/J.Tetlet.2014.10.063 |
0.336 |
|
2012 |
Beng TK, Tyree WS, Parker T, Su C, Williard PG, Gawley RE. Dynamics of catalytic resolution of 2-lithio-N-Boc-piperidine by ligand exchange. Journal of the American Chemical Society. 134: 16845-55. PMID 22967289 DOI: 10.1021/Ja307796E |
0.553 |
|
2012 |
Beng TK, Woo JS, Gawley RE. Synthetic applications and inversion dynamics of configurationally stable 2-lithio-2-arylpyrrolidines and -piperidines. Journal of the American Chemical Society. 134: 14764-71. PMID 22881214 DOI: 10.1021/Ja306276W |
0.689 |
|
2012 |
Beng TK, Gawley RE. CATALYTIC DYNAMIC RESOLUTION APPLIED TO THE SYNTHESIS OF 2,6-DISUBSTITUTED PIPERIDINES: PREPARATION OF (+)-LUPETIDINE AND (-)-EPIDIHYDROPINIDINE. Heterocycles. 84: 697-718. PMID 22408286 DOI: 10.3987/Com-11-S(P)45 |
0.695 |
|
2011 |
Beng TK, Gawley RE. Application of catalytic dynamic resolution of N-Boc-2-lithiopiperidine to the asymmetric synthesis of 2-aryl and 2-vinyl piperidines. Organic Letters. 13: 394-7. PMID 21174392 DOI: 10.1021/Ol102682R |
0.726 |
|
2010 |
Beng TK, Gawley RE. Highly enantioselective catalytic dynamic resolution of N-Boc-2-lithiopiperidine: synthesis of (R)-(+)-N-Boc-pipecolic acid, (S)-(-)-coniine, (S)-(+)-pelletierine, (+)-beta-conhydrine, and (S)-(-)-ropivacaine and formal synthesis of (-)-lasubine II and (+)-cermizine C. Journal of the American Chemical Society. 132: 12216-7. PMID 20806976 DOI: 10.1021/Ja105772Z |
0.666 |
|
2009 |
Coldham I, Leonori D, Beng TK, Gawley RE. The barrier to enantiomerization and dynamic resolution of N-Boc-2-lithiopiperidine and the effect of TMEDA. Chemical Communications (Cambridge, England). 5239-41. PMID 19707632 DOI: 10.1039/B911024K |
0.743 |
|
2009 |
Beng TK, Yousaf TI, Coldham I, Gawley RE. Enantiomerization dynamics and a catalytic dynamic resolution of N-trimethylallyl-2-lithiopyrrolidine. Journal of the American Chemical Society. 131: 6908-9. PMID 19405472 DOI: 10.1021/Ja900755A |
0.712 |
|
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