Výsledky vyhledávání - "Hanmanth Reddy Vulupala"

A convenient synthesis and screening of benzosuberone bearing 1,2,3-triazoles against Mycobacterium tuberculosis

Autor: Lavanya Jilla, Yasodakrishna Sajja, Sowmya Vanguru, Dharmarajan Sriram, Perumal Yogeswari, Hanmanth Reddy Vulupala, Rajashaker Bantu, Lingaiah Nagarapu

Publikováno v: Bioorganic & Medicinal Chemistry Letters. 26:4292-4295

A series of benzosuberone bearing 1,2,3-triazoles were rationally designed and alkyl/aryl groups appended on 1,2,3-triazole derivatives 5a-o were synthesized using click chemistry and evaluated for their in vitro antimycobacterial activity against My

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e3fd689d1c70daba2a992d319783f14
https://doi.org/10.1016/j.bmcl.2016.07.039

Zobrazit plný text záznamu

Potent ACE inhibitors from 5-hydroxy indanone derivatives

Autor: Lingaiah Nagarapu, Sanjay K. Benerjee, Hanmanth Reddy Vulupala, Yasodakrishna Sajja, Raviteja Bandla, Pankaj K. Bagul

Publikováno v: Bioorganic chemistry. 77

A novel triazole derivatives(±)-2-(hydroxymethyl)-7,8-dihydro-1H-indeno[5,4-b]furan-6(2H)-one (12a–j) were designed and synthesized by the reaction between racemic azide and terminal acetylenes under click chemistry reaction conditions followed by

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d5729bf83c30d25610f6a085e66c6c7
https://pubmed.ncbi.nlm.nih.gov/29502027

Zobrazit plný text záznamu

Design, synthesis and in vitro anti-tuberculosis activity of benzo[6,7]cyclohepta[1,2-b]pyridine-1,2,3-triazole derivatives

Autor: Dharmarajan Sriram, Hanmanth Reddy Vulupala, Rajashaker Bantu, Yasodakrishna Sajja, Sowmya Vanguru, Perumal Yogeswari, Lingaiah Nagarapu

Publikováno v: Bioorganicmedicinal chemistry letters. 27(23)

A series of novel benzo[6,7]cyclohepta[1,2-b]pyridine-1,2,3-triazole hybrids (7a–j & 8a–j) have been designed and synthesized in excellent yields by Huisgen’s [3+2] cyclo addition reaction of 3-(azidomethyl)-2-methyl-6,7-dihydro-5H-benzo[6,7]cy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a5208e20b9cfa91245100455695c739
https://pubmed.ncbi.nlm.nih.gov/29113761

Zobrazit plný text záznamu

Efficient synthesis and resolution of novel 2-(hydroxymethyl)-7,8-dihydro-1H-indeno[5,4-b] furan-6(2H)-one by lipase Pseudomonas cepacia

Autor: Yashodakrishna Sajja, Hanmanth Reddy Vulupala, Jagadeesh Babu Nanubolu, Rajashaker Bantu, Lingaiah Nagarapu

Publikováno v: Tetrahedron: Asymmetry. 25:578-582

Lipase Pseudomonas cepacia catalyzed acylation of (±)-2-(hydroxymethyl)-7,8-dihydro-1H-indeno[5,4-b] furan-6(2H)-one using vinyl acetate as the acyl donor in acetone gave (−)-(R)-2-acetoxy-2-(methyl)-7,8-dihydro-1H-indeno[5,4-b] furan-6(2H)-one an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7a1dda8fab621106d6f3b68480ebc7d9
https://doi.org/10.1016/j.tetasy.2014.02.008

Zobrazit plný text záznamu

Design, synthesis, and in vitro antituberculosis activity of benzo[6,7]cyclohepta[1,2-b]pyridine-1,3,4-oxadiazole derivatives

Autor: Dharmarajan Sriram, Jagadeesh Babu Nanubolu, Hanmanth Reddy Vulupala, Sowmya Vanguru, Lingaiah Nagarapu, Yasodakrishna Sajja, Yogeswari Perumal

Publikováno v: Chemical biologydrug design. 90(4)

A new antitubercular agents, benzo[6,7]cyclohepta[1,2-b]pyridine-1,3,4- oxadiazole hybrids (6a–o), have been designed and synthesized involving oxidative cyclization of hydrazones by use of di(acetoxy)iodobenzene, characterized by IR,1H NMR,13C NMR

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b57ad525795cb39913beed52b6774577
https://pubmed.ncbi.nlm.nih.gov/28267891

Zobrazit plný text záznamu

Molecular Iodine–Catalyzed Synthesis of 1,2,3,6-Tetrahydropyrimidines

Autor: Lingaiah Nagarapu, Hanmanth Reddy Vulupala, Rajashaker Bantu, Ch. Venkatanarsimhaji, A. Ramakrishna Reddy

Publikováno v: Synthetic Communications. 42:2131-2138

A short and simple synthesis of tetrahydropyrimidine derivatives were accomplished in good to excellect yields at room temperature by the reaction of dimethylacetalynedicarboxylate, aniline, and formaldehyde in the presence of 5 mol% of molecular iod

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0968029f14234615a5a621800a6bfb60
https://doi.org/10.1080/00397911.2011.554061

Zobrazit plný text záznamu

Plný text ve formátu HTML

Three-component, one-pot synthesis of benzo[6,7]cyclohepta[1,2-b]pyridine derivatives under catalyst free conditions and evaluation of their anti-inflammatory activity

Autor: Sathish Babu Vasamsetti, Hanmanth Reddy Vulupala, Rajashaker Bantu, Srigiridhar Kotamraju, Jagadeesh Babu Nanubolu, Lingaiah Nagarapu, Yasodakrishna Sajja

Publikováno v: Bioorganicmedicinal chemistry letters. 26(3)

An efficient three-component protocol is described for the synthesis of benzo[6,7]cyclohepta[1,2-b]pyridine derivatives using β-chloroacroleins, 1,3-dicarbonyls and ammonium acetate under catalyst free conditions by using ethanol as reaction media.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f11f395a579cdf358b0292c073a1bbc
https://pubmed.ncbi.nlm.nih.gov/26748696

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání