Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Panduga Ramaraju"'
Akademický článek
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Akademický článek
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Akademický článek
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Autor:
Gavinolla, Vijayalaxmi, Thangalipalli, Swathi, Bandalla, Siddarama Goud, Panduga, Ramaraju, Neella, Chandra Kiran
Publikováno v:
New Journal of Chemistry; 12/7/2023, Vol. 47 Issue 45, p20777-20784, 8p
Autor:
Satheeshvarma Vanaparthi, Rajpal Singh, Nisar A. Mir, Sachin Choudhary, Panduga Ramaraju, Rajnish Prakash Singh, Preetika Sharma, Indresh Kumar, Murugesan Sankaranarayanan, Rajni Kant
Publikováno v:
New Journal of Chemistry. 44:16329-16339
A sequential multicomponent synthesis of highly substituted pyrrole-3-carboxaldehydes has been developed under metal-free conditions. This one-pot protocol involves proline-catalyzed direct chemoselective Mannich reaction-cyclization between 1,4-keto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fb0ab9685fe8010c3efc0e62aba4f79
https://doi.org/10.1039/d0nj03575k
https://doi.org/10.1039/d0nj03575k
Autor:
Rajni Kant, Amol Prakash Pawar, Nisar A. Mir, Sachin Choudhary, Indresh Kumar, Devinder Kumar Sharma, Panduga Ramaraju, Eldhose Iype
Publikováno v:
The Journal of Organic Chemistry. 84:12408-12419
A pot-economic method for the enantio- and diastereoselective synthesis of a [2.2.2] azabicyclic isoquinuclidine system is developed. This protocol involves the proline-catalyzed direct Mannich rea...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b398fbb3445ef882f49db5d73d533b1d
https://doi.org/10.1021/acs.joc.9b01865
https://doi.org/10.1021/acs.joc.9b01865
Publikováno v:
Organic Letters. 20:1023-1026
The first catalytic enantioselective nitroso aldol reaction of distal dialdehydes is reported. The reaction is catalyzed by simple l-proline at room temperature and subsequent reduction delivered biologically potent and synthetically versatile N–O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c21ee38f451b0dc4c18cec40d0dbcaf
https://doi.org/10.1021/acs.orglett.7b03968
https://doi.org/10.1021/acs.orglett.7b03968
Publikováno v:
European Journal of Organic Chemistry. 2017:3461-3465
A new method for the direct one-pot synthesis of substituted pyrrole-2,4-dialdehdyes is developed. This overall pseudo-[3+2] annulation reaction between glutaraldehyde and N-PMP-aldimines (PMP = p-OMeC6H4) proceed through proline-catalyzed direct Man
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::686122fc74abb3ab0c9b1225ddb8c8f2
https://doi.org/10.1002/ejoc.201700500
https://doi.org/10.1002/ejoc.201700500
Autor:
Panduga, Ramaraju, Amol Prakash, Pawar, Eldhose, Iype, Nisar A, Mir, Sachin, Choudhary, Devinder Kumar, Sharma, Rajni, Kant, Indresh, Kumar
Publikováno v:
The Journal of organic chemistry. 84(19)
A pot-economic method for the enantio- and diastereoselective synthesis of a [2.2.2] azabicyclic isoquinuclidine system is developed. This protocol involves the proline-catalyzed direct Mannich reaction-cyclization/IBX-mediated site-selective oxidati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::67d8aadcb46c693123d9626f82b02f19
https://pubmed.ncbi.nlm.nih.gov/31486644
https://pubmed.ncbi.nlm.nih.gov/31486644
Publikováno v:
RSC Advances. 6:60422-60432
An enantioselective multi-component synthesis of 1,2,5,6-tetrahydropyridines (THPs) has been developed through a one-pot domino-process. This transformation proceeds through proline-catalyzed direct Mannich reaction-cyclization of glutaraldehyde with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b0d4a0832cadd838243e03030386702
https://doi.org/10.1039/c6ra12965j
https://doi.org/10.1039/c6ra12965j