A Venkateswarlu
Overview
Explore the profile of A Venkateswarlu including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
49
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0
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Recent Articles
1.
Subba Reddy B, Venkateswarlu A, Sridevi B, Aldeyab S, Vinu A
J Nanosci Nanotechnol
. 2015 Dec;
15(9):6826-32.
PMID: 26716251
Friedel-Crafts alkylation of electron-rich arenes with aldehydes has been achieved in the presence of an active and selective Amberlyst-15 catalyst at the reaction temperature of 60 degrees C in solvent-free...
2.
Venkateswarlu A, Kanakaraju M, Kunwar A, Subba Reddy B
Org Biomol Chem
. 2015 Aug;
13(40):10212-5.
PMID: 26308943
Aldehydes undergo a smooth coupling with (E/Z)-non-3-en-8-yn-1-ol in the presence of 10 mol% of CuX and BF3·OEt2 under mild conditions to produce a novel class of octahydrocyclohepta[c]pyran-6(1H)-one derivatives in good...
3.
Kamal A, Subba Reddy B, Sridevi B, Ravikumar A, Venkateswarlu A, Sravanthi G, et al.
Bioorg Med Chem Lett
. 2015 Aug;
25(18):3867-72.
PMID: 26253635
Natural alkaloid, tryptanthrin (indolo[2,1-b]quinazoline-6,12-dione) and its analogues are found to exhibit potent anti-tubercular activity against MDR-TB. A novel class of indolo[2,1-b]quinazolinones have been synthesized to evaluate their anti-mycobacterial activity. Enoyl-acyl...
4.
Subba Reddy B, Venkateswarlu A, Sridevi B, Marumudi K, Kunwar A, Gayatri G
Org Biomol Chem
. 2015 Mar;
13(14):4351.
PMID: 25760798
No abstract available.
5.
Subba Reddy B, Venkateswarlu A, Sridevi B, Marumudi K, Kunwar A, Gayatri G
Org Biomol Chem
. 2015 Jan;
13(9):2669-72.
PMID: 25582106
E- and Z-9-Methyldeca-3,8-dien-1-ols undergo smooth cyclization with aldehydes in the presence of 20 mol% AgSbF6 under extremely mild conditions to generate the corresponding oxa-bicycles in good yields with excellent selectivity....
6.
Subba Reddy B, Venkateswarlu A, Borkar P, Yadav J, Sridhar B, Gree R
J Org Chem
. 2014 Feb;
79(6):2716-22.
PMID: 24564269
An unprecedented oxa- versus thia-selectivity has been observed in Prins cyclization of 6-mercaptohex-3-en-1-ol with aldehydes. In the presence of a stoichiometric amount of strong Lewis or Brønsted acids, the reaction...
7.
Subba Reddy B, Venkateswarlu A, Borkar P, Yadav J, Kanakaraju M, Kunwar A, et al.
J Org Chem
. 2013 May;
78(12):6303-8.
PMID: 23679080
A novel thia-Prins bicyclization approach has been developed for the first time for the synthesis of hexahydro-2H-thieno[3,2-c]thiopyran derivatives from the coupling of homoallylic mercaptans such as hex-3-ene-1,6-dithiol with various aldehydes...
8.
Singh S, Reddy P, Rao K, Lohray B, Misra P, Rajjak S, et al.
Bioorg Med Chem Lett
. 2003 Dec;
14(2):499-504.
PMID: 14698190
Several chemical modifications in the N(1)-benzenesulfonamide ring of celecoxib are presented. The series with a hydroxymethyl group adjacent to the sulfonamide was found to be the most potent modification that...
9.
Sharma V, Adi Seshu K, Sekhar V, Madan S, Vishnu B, Babu P, et al.
Bioorg Med Chem Lett
. 2003 Dec;
14(1):67-71.
PMID: 14684300
A new series of [4-(2-phenylethenesulfonylmethyl)phenyl]quinazolin-4-yl-amines was prepared and tested for its in vitro cytotoxic activity against a panel of 12 human cancer cell lines. Compounds 9, 15, 24 and 31...
10.
Nanduri S, Thunuguntla S, Nyavanandi V, Kasu S, Mahesh Kumar P, Sai Ram P, et al.
Bioorg Med Chem Lett
. 2003 Nov;
13(22):4111-5.
PMID: 14592518
Azadirone 1, a limonoidal constituent of Azadirachta indica is found to possess potent cytotoxic activity against a panel of human cancer cell lines in our in vitro studies. In vitro...