Zobrazeno 1 - 10
of 40
pro vyhledávání: '"N Mallikarjuna Reddy"'
Publikováno v:
ChemistrySelect. 4:4726-4730
Publikováno v:
International Journal of Integrative Medical Sciences. 2:79-86
Publikováno v:
International Journal of Integrative Medical Sciences. 2:61-69
61 Original Article Role of Oxidative Stress on Age and Gender Sailaja M. V *1, Sharan B. Singh M 2, Ch. Rajendhra 3, N. Mallikarjuna Reddy 4. *1 Assistant Professor, Dept. of Physiology, RIMS, Kadapa, Andhra Pradesh, India. 2 Professor, Dept of Phys
Autor:
N. Mallikarjuna Reddy
Publikováno v:
Operative Atlas of Laparoscopic and Robotic Reconstructive Urology ISBN: 9783319332291
Following the introduction of clean self intermittent catheterization (CSIC) by Jack Lapides which revolutionized bladder drainage; many modifications have been done to achieve this. One popular technique is the Mitrofanoff procedure, using appendix
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f20a0f35ae908b4bd5b5f82bd700f8e4
https://doi.org/10.1007/978-3-319-33231-4_43
https://doi.org/10.1007/978-3-319-33231-4_43
Publikováno v:
European Journal of Organic Chemistry. 2014:5574-5581
The stereoselective synthesis of the spiroketal fragment of the immunosuppressant (–)-ushikulide A is described. The salient feature of this synthesis is the construction of the spiroketal moiety by hydrolysis of a dialkylated tosylmethyl isocyanid
Autor:
N. Mallikarjuna Reddy, Md. Ataur Rahman, Attaluri R. Prasad, Jhillu S. Yadav, Ahmad Al Khazim Al Ghamdi
Publikováno v:
Synlett. 25:661-664
The stereoselective total synthesis of rhoiptelol B, a diarylheptanoid isolated from Rhoiptelea chiliantha is described. The tetrahydropyran ring was constructed by using Prins cyclization. The key steps involved in this synthesis are Prins cycliza
Publikováno v:
Tetrahedron Letters. 56:365-367
An asymmetric synthesis of spiroketal fragment of an antitumour antibiotic, ossamycin is described. Coupling of aldehyde and alkyne fragments followed by spiroketalization has afforded the spiroketal sub unit of ossamycin. Both the sub targets were c
Publikováno v:
Tetrahedron. 69:8618-8625
The stereoselective total synthesis of (−)-brevisamide, a novel marine cyclic ether alkaloid isolated from dinoflagellate karenia brevis is described. The key steps involved in this synthesis are the Sharpless asymmetric epoxidation and regioselect
Publikováno v:
International Journal of Medical Research and Health Sciences, Vol 2, Iss 4, Pp 724-729 (2013)
Objectives: we found only effects of at least a short term practice extended over a period of a few days to weeks of pranayama (alternate nostril breathing) rather than acute effects of unilateral right nostril breathing (suryanadi pranayama). Keepin
Autor:
Jhillu S. Yadav, K. Anantha Lakshmi, A. Ramachandra Prasad, N. Swapnil, N. Mallikarjuna Reddy
Publikováno v:
Tetrahedron: Asymmetry. 23:1155-1160
The stereoselective total synthesis of decarestrictine O, a polyketide natural product is described. The synthesis involves MacMillan α-hydroxylation, C1-Wittig olefination, hydrolytic kinetic resolution and ring closing metathesis (RCM) as key step