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Prashant Kumar, PhD Profile
Prashant Kumar, PhD

@0kumarprashant

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217
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2
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126

PhD (@IiserMohali), Postdoc (@queensu, @QueensChem)

Joined February 2020
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@0kumarprashant
Prashant Kumar, PhD
28 days
ATROPISOMERIC INDENES through asymmetric palladium-catalyzed Suzuki–Miyaura cross-coupling reactions @J_A_C_S . This work underscores the importance of axially chiral indenes and addresses a notable gap in the field. Many congratulations to the authors! 👏
@J_A_C_S
J. Am. Chem. Soc.
29 days
Atropisomeric Indene (AroInd) Libraries: Design, Catalytic Synthesis, and Applications | Journal of the American Chemical Society
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@J_A_C_S
J. Am. Chem. Soc.
29 days
Atropisomeric Indene (AroInd) Libraries: Design, Catalytic Synthesis, and Applications | Journal of the American Chemical Society
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pubs.acs.org
The development of chiral indenyl metal complexes has been hindered by inefficient synthetic methods, significantly lagging behind the well-established Cp metal complexes. In this study, we present a...
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@athavale_s
Soumitra Athavale
1 month
Thrilled to share the first paper from our group at UCLA, online today in Science: “Biocatalytic, Asymmetric Radical Hydrogenation of Unactivated Alkenes” @uclachem @ScienceMagazine https://t.co/YCtGp91kd2
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science.org
Alkene hydrogenation is a cornerstone of chemical synthesis, yet enzymatic strategies remain limited to electron deficient substrates via hydride transfer. Using heme enzymes, we unlock a hydrogena...
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@MJKoh87
MJ Koh Group
1 month
Atom-swapping in a saturated heterocycle? We report a photocatalytic transmutation strategy in @Nature that exchanges O within an oxetane for N, S, C & even dual atoms, simplifying access to a variety of non-aromatic cyclic pharmacophores & enabling late-stage editing of complex
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@AB_Group_IISER
AB Research Group
3 months
Happy to share our recent #OrgLett. article on 'Asymmetric @totalsynthesis of (+)-shearilicine'. Congratulations to @NandaKisho34936 @ranjitmurmu0015 @MOUMITA23914029 @SouvikBisw76894 Read the article here: https://t.co/1v5Ixgzlpf
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@MartinTomanik
Martin Tomanik
3 months
Out today in @J_A_C_S is the first synthesis from our group!! We report a convergent and stereoselective total synthesis of the nominal structure of Talaromyolide D. Huge congrats to Bo and Alex! @nyuchemistry @TotalSynthesis https://t.co/1MJBXeBXmc
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@basker25071980
Basker Sundararaju
4 months
Check out our @J_A_C_S on accessing chiral C–N axes under cobalt catalysis! Congrats to @iamAbirdas @maity_pritam02 Kumaran & @Richard_UKT for DFT Thanks to @IFCPAR for funding & @iitkanpur for infra shout out to lab @Basker_IITK @Chemistry_IITK @director_iitk #asymmetric
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@0kumarprashant
Prashant Kumar, PhD
5 months
Interesting!! Further development involving benzylic gem-diacetates in Pd catalysis. Previously demonstrated in our work:
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pubs.acs.org
Unlike that of benzyl acetates, the chemistry of benzyl gem-diacetates is rarely explored under metal catalysis. Here, we describe the first palladium-catalyzed cascade annulative allylic alkylation...
@ChemistryNews
Chemistry News
5 months
Stereodivergent synthesis of benzylic alcohol derivatives enabled by Pd/Cu co-catalyzed asymmetric benzylic substitution reaction https://t.co/yuAtHTAS42
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@EngleLab
Engle Lab
6 months
atropisomers? positional isomers? both? We present beautiful and curious class of molecules today in @ChemRxiv. 🧐🪞 https://t.co/76QEU36cr3 @ASimlandy @0iTurki @pengliu_group
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@0kumarprashant
Prashant Kumar, PhD
6 months
Fascinating work! Elegant and fundamental strategy for accessing versatile axially chiral styrene precursors
@EngleLab
Engle Lab
6 months
atropisomers? positional isomers? both? We present beautiful and curious class of molecules today in @ChemRxiv. 🧐🪞 https://t.co/76QEU36cr3 @ASimlandy @0iTurki @pengliu_group
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@UyedaLab
Uyeda Lab
6 months
Our latest nickel catalysis paper is out now in JACS ASAP! See Wen, Calvin, and Will's (in collaboration with Professor Christina Li) work on terpene alkaloid natural product synthesis through [4+1]-cycloaddition below! 🧪 https://t.co/u4vDyNsnrS
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pubs.acs.org
Intramolecular Diels–Alder reactions are privileged strategic disconnections in the synthesis of polycyclic natural products containing six-membered rings. The analogous [4 + 1]-cycloaddition may...
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@IiserMohali
IISER Mohali
7 months
Salute to the Indian Armed Forces and its brave soldiers for successful execution of #OperationSindoor 🫡 It reflects India's unwavering commitment to national security. #IndianArmy #NationFirst @EduMinOfIndia
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@TotalSynthesis
Total Synthesis
7 months
Concise Enantioselective #TotalSyntheses of Rearranged ent-Trachylobane Diterpenoids (–)-Wallichanols A and B by Dattatraya H. Dethe, Nitin Sharma, and Sakshi Juyal in @angew_chem https://t.co/DDtoifoaBO
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@J_A_C_S
J. Am. Chem. Soc.
8 months
Empowering Diastereoselective Cyclopropanation of Unactivated Alkenes with Sulfur Ylides through Nucleopalladation | Journal of the American Chemical Society @iitmadras @TotalSyntheses @JainDeemedtbUnv
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pubs.acs.org
Regio- and stereoselective cyclopropanation of unactivated alkenes under mild conditions remains a challenging yet fundamental transformation. We present a versatile palladium(II)-catalyzed method...
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@HariGroupIISc
The Hari Group
1 year
Our work on the first sigmatropic rearrangement with [1.1.1]propellane for accessing functionalized MCBs and its application in the synthesis of BCHs is out @ChemRxiv. Thanks, @serbonline @iiscbangalore, for the funding. https://t.co/szLAwjKeW4
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@FerozAh49503387
Feroz Ahmad
1 year
Check out our recent work published in @JOC_OL @acs Domino Approach to Heterocycles-Based Unsymmetrical Triarylmethanes through Heteroannulation of 2‑(2-Enynyl)pyridines with Enaminones. From @RVijayaAnand1 Lab @DCS_IISERMOHALI https://t.co/TUfKqxjp0G
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pubs.acs.org
Herein, we report a copper-catalyzed protocol to access unsymmetrical triarylmethanes containing both indolizine and the chromone scaffolds in the same molecule via a 5-endo-dig cyclization of...
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@LuptonChemistry
LuptonChem
1 year
Congratulations to Toni, Jeremy, Jing and @BreugstLab for our recent @angew_chem An unusual 2C enantioselective annulation possible by rethinking how this intermediate is accessed using phosphine organicatalysis. https://t.co/paazUZFEV1
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onlinelibrary.wiley.com
Vinylphosphonium intermediates, commonly accessed from ynoates, undergo normal and reverse polarity couplings. Herein we exploit β-iodoenoates as alternatives to ynoates. As a consequence, we have...
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