Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Kanakaraju, Marumudi."'
Autor:
Adepu, Ramesh, Kanakaraju, Marumudi, Chandramouli, Nagula, Reddy, Purushotham P., Sharma, Gangavaram V.M., Sarma, Akella V.S., Kunwar, Ajit C.
Publikováno v:
In Tetrahedron 18 October 2018 74(42):6095-6106
Synthesis of new β2,2-amino acids with carbohydrate side chains: impact on the synthesis of peptides
Autor:
Sharma, Gangavaram V.M., Rajender, Karnekanti, Sridhar, Gattu, Reddy, Post Sai, Kanakaraju, Marumudi
Publikováno v:
In Carbohydrate Research 31 March 2014 388:8-18
Autor:
Kanakaraju Marumudi, Shivalal Banoth, Utkal Mani Choudhury, Debendra K. Mohapatra, Ajit C. Kunwar
Publikováno v:
Synlett. 32:685-688
A concise and convergent stereoselective synthesis of curvulone B is described. The synthesis utilized a tandem isomerization followed by C–O and C–C bond-forming reactions following Mukaiyama-type aldol conditions for the construction of the tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d46706e7d67b76b8719dc809c622211
https://doi.org/10.1055/a-1297-6838
https://doi.org/10.1055/a-1297-6838
Autor:
Kanakaraju Marumudi, Janardhan Gaddam, Debendra K. Mohapatra, Jhillu S. Yadav, G. Sudhakar Reddy, Ajit C. Kunwar
Publikováno v:
Organic & Biomolecular Chemistry. 17:5601-5614
The first asymmetric total synthesis and stereochemical assignments of 10-membered macrolactones relgro and 10'-oxorelgro are disclosed. To this end, palladium-catalyzed Stille coupling, the Mitsunobu reaction, ring-closing metathesis, EDCI promoted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1151f9f74589124440e6de25851675c0
https://doi.org/10.1039/c9ob00838a
https://doi.org/10.1039/c9ob00838a
Autor:
Abdullah Alarifi, Ahmed Kamal, Syed Mohammed Ali Hussaini, B. Sridevi, Faria Sultana, Siddiq Pasha Shaik, Debanjan Bhattacharjee, Vadithe Lakshma Nayak, Kanakaraju Marumudi, Thokhir Basha Shaik
Publikováno v:
ChemistrySelect. 2:9901-9910
A series of 2-anilinopyridyl linked oxindole conjugates (6 a-ad) were synthesized andevaluated for their antiproliferative activity against a panel of four human cancer cell lines viz., HeLa, DU-145, A549 and MCF-7. All the compounds showed very good
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff54e07500bda49c8e279e51007eeb26
https://doi.org/10.1002/slct.201701787
https://doi.org/10.1002/slct.201701787
Autor:
Debendra K. Mohapatra, Kanakaraju Marumudi, Ajit C. Kunwar, Jhillu S. Yadav, Suresh Kanikarapu
Publikováno v:
Organic Letters. 19:4167-4170
The first asymmetric total synthesis of two possible diastereomers (4S,5R)-4,8-dihydroxy-3,4-dihydrovernoniyne 5 and (4S,5S)-4,8-dihydroxy-3,4-dihydrovernoniyne 5a is accomplished. Salient features of the synthesis involve Cadiot–Chodkiewicz coupli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a064c98d02d46f66ad457cb7200cb948
https://doi.org/10.1021/acs.orglett.7b01620
https://doi.org/10.1021/acs.orglett.7b01620
Autor:
Kanakaraju Marumudi, Debendra K. Mohapatra, J. S. Yadav, Ajit C. Kunwar, Suresh Kanikarapu, Saurabh Maity
Publikováno v:
The Journal of Organic Chemistry. 82:4561-4568
The first asymmetric total synthesis of the putative structure of diplopyrone was achieved in 17 linear steps starting from cis-1,4-butene-diol. The synthetic route features iodine-catalyzed tandem isomerization followed by C–O and C–C bond forma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3d6569cd453256f0207bad4098dda95
https://doi.org/10.1021/acs.joc.7b00086
https://doi.org/10.1021/acs.joc.7b00086
Publikováno v:
Organic Letters. 19:1642-1645
Conversion of vinyl pyranosylamine and vinyl furanosylamines to 2,6- and 2,5-disubstituted pyrrolidine and piperidine iminosugars, respectively, in one pot was developed using Kimura and Tamaru’s procedure, where a Pd salt in the presence of Et2Zn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0c75d7d25bc6c7f5f14f9deda581ab9
https://doi.org/10.1021/acs.orglett.7b00441
https://doi.org/10.1021/acs.orglett.7b00441
Autor:
Venkateswarlu, Anipireddy1, Kanakaraju, Marumudi.2, Kunwar, Ajit C.2, Rami Reddy, Yellala V.3, Reddy, Basi V. S.1 basireddy@iict.res.in
Publikováno v:
European Journal of Organic Chemistry. Aug2015, Vol. 2015 Issue 24, p5389-5392. 4p.
Autor:
N. Prudhvi Raju, B. Jagan Mohan Reddy, A. C. Kunwar, B. Someswarao, Kanakaraju Marumudi, B. Sridhar, B. V. Subba Reddy
Publikováno v:
Organic & Biomolecular Chemistry. 13:4733-4736
A novel bicyclization of 2-(2-(hydroxymethyl)-1-methylene-2,3-dihydro-1H-inden-2-yl)ethanol with aldehydes in the presence of 10 mol% BF3·OEt2 in dichloromethane at 0-25 °C affords the biologically relevant indeno[2,1-c]pyran scaffolds in good yiel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a752345f5447db053fdaacc9328ac553
https://doi.org/10.1039/c5ob00376h
https://doi.org/10.1039/c5ob00376h