Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Mandalaparthi Phanindrudu"'
Publikováno v:
Chemical Communications. 59:3795-3811
Prochiral 2,5-cyclohexadienones, being stable and easily accessible, are privileged key building blocks for the synthesis of complex molecules and bioactive natural products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef900ea95334bfcc5180d51811e93aa9
https://doi.org/10.1039/d3cc00509g
https://doi.org/10.1039/d3cc00509g
Publikováno v:
The Chemical Record. 21:3689-3726
The development of transition-metal catalyzed enantioselective and diastereoselective transformations has contributed many advances in the field of synthetic organic chemistry. Particularly, stereoselective desymmetrization of prochiral cyclohexadien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::078d7f2910ab7f1ee0388d7787ff0293
https://doi.org/10.1002/tcr.202100136
https://doi.org/10.1002/tcr.202100136
Autor:
Jagadeesh Babu Nanubolu, Ahmed Kamal, Budaganaboyina Prasad, Mandalaparthi Phanindrudu, Dharmendra Kumar Tiwari
Publikováno v:
Chemical Communications. 57:9542-9545
Here in the present manuscript, we report our observation of an unprecedented stereoselective synthesis of 2H-isoindolin-1,3-ylidenes from 2-(formylphenyl)acrylates and phenacylazide in the presence of piperidine. Unlike in our previous findings, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05e68635392638facfd1a7c501ae54bf
https://doi.org/10.1039/d1cc02884g
https://doi.org/10.1039/d1cc02884g
Autor:
Satenik Mkrtchyan, Mohanad Shkoor, Mandalaparthi Phanindrudu, Miroslav Medved′, Olena Sevastyanova, Viktor O. Iaroshenko
The amide bond is prominent in natural and synthetic organic molecules endowed with activity in various fields. Among a wide array of amide synthetic methods, substitution on a pre-existing (O)C-N moiety is an underexplored strategy for the synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9b770d7ae242b41375b3f8ee82d09df
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85146130268&origin=inward
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85146130268&origin=inward
Autor:
Budaganaboyina, Prasad, Mandalaparthi, Phanindrudu, Jagadeesh Babu, Nanubolu, Ahmed, Kamal, Dharmendra Kumar, Tiwari
Publikováno v:
Chemical communications (Cambridge, England). 57(75)
Here in the present manuscript, we report our observation of an unprecedented stereoselective synthesis of 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6e1417055f72c1e4c4bd097eea4a7429
https://pubmed.ncbi.nlm.nih.gov/34546244
https://pubmed.ncbi.nlm.nih.gov/34546244
Publikováno v:
The Journal of Organic Chemistry. 84:12334-12343
An efficient and transition-metal-free strategy for the synthesis of 3-keto-isoquinolines in one pot has been developed from the easily accessible 2-(formylphenyl)acrylates and phenacyl azides. Various substituted aldehydes and phenacyl azides were s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::196d052d99845668787971f3003f0279
https://doi.org/10.1021/acs.joc.9b01534
https://doi.org/10.1021/acs.joc.9b01534
Autor:
Pushpendra, Dharmendra Kumar Tiwari, Dipak Kumar Tiwari, Sandip Balasaheb Wakade, Mandalaparthi Phanindrudu
Publikováno v:
Tetrahedron. 75:4024-4030
An efficient and transition metal-free approach for the synthesis of functionalized 3-ketoquinolines from readily available anilines, enaminones and DMSO in the presence of K2S2O8 has been conducted. This one pot tandem reaction proceeds through [3+2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e95b620c126d01cd6bf22ba37602f893
https://doi.org/10.1016/j.tet.2019.06.030
https://doi.org/10.1016/j.tet.2019.06.030
Autor:
Dharmendra Kumar Tiwari, Dipak Kumar Tiwari, Mandalaparthi Phanindrudu, Pravin R. Likhar, Sandip Balasaheb Wakade
Publikováno v:
The Journal of Organic Chemistry. 83:9137-9143
An efficient and transition-metal-free approach for the synthesis of 4-arylquinolines from readily available anilines and alkynes in the presence of K2S2O8 and DMSO has been developed. A variety of alkynes and anilines having a diverse range of subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45194e5834451b0f754456fdecd8a00d
https://doi.org/10.1021/acs.joc.8b01204
https://doi.org/10.1021/acs.joc.8b01204
Autor:
Pothapragada S. K. Prabhakar Ganesh, Mandalaparthi Phanindrudu, Sandip Balasaheb Wakade, Pravin R. Likhar, Dharmendra Kumar Tiwari, Dipak Kumar Tiwari
Publikováno v:
Organic Letters. 19:4948-4951
A transition-metal-free method for the construction of functionalized quinolines from readily available acetophenones and anthranils is reported. This one-pot reaction cascade involves in situ generation of α,β-unsaturated ketones from the acetophe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e9cbcd1c735ee1cf33a4d5e041ae8fd
https://doi.org/10.1021/acs.orglett.7b02429
https://doi.org/10.1021/acs.orglett.7b02429
Autor:
Dharmendra Kumar Tiwari, Sandip Balasaheb Wakade, Dipak Kumar Tiwari, Jagadeesh Babu Nanubolu, Mandalaparthi Phanindrudu
Publikováno v:
Chemical Communications. 53:5302-5305
An efficient method to access functionalized quinolines from the readily available saturated ketones and anthranils has been explored. This one-pot cascade reaction involves the in situ generation of α,β-unsaturated ketones by the copper catalysed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e90d436944632625509af08338672e84
https://doi.org/10.1039/c7cc01195d
https://doi.org/10.1039/c7cc01195d