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Boyapelly, Kumaraswamy
9
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Online (9)
Mediatypes
Articles (Online) (7)
OpenAccess-fulltext (2)
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1
Rationally Designed Pyrimidine Compounds: Promising Novel A..:
Millette, Guillaume
;
Lacasse, Evelyne
;
Binette, Renaud
...
Antibiotics. 12 (2023) 8 - p. 1344 , 2023
Link:
https://doi.org/10.3390/..
?
2
Purine analogs targeting the guanine riboswitch as potentia..:
Yan, Lok-Hang
;
Le Roux, Antoine
;
Boyapelly, Kumaraswamy
...
European Journal of Medicinal Chemistry. 143 (2018) - p. 755-768 , 2018
Link:
https://doi.org/10.1016/..
?
3
Synthesis and Characterization of a Phosphate Prodrug of Is..:
Boyapelly, Kumaraswamy
;
Bonin, Marc-André
;
Traboulsi, Hussein
...
Journal of Natural Products. 80 (2017) 4 - p. 879-886 , 2017
Link:
https://doi.org/10.1021/..
?
4
A simple and efficient synthesis of goniothalesdiol A:
Thakur, Pallavi
;
Boyapelly, Kumaraswamy
;
Gurram, Raji Reddy
..
Tetrahedron: Asymmetry. 23 (2012) 9 - p. 659-661 , 2012
Link:
https://doi.org/10.1016/..
?
5
Stereoselective Total Synthesis of (+)-Oploxyne A, (−)-Oplo..:
Yadav, J. S.
;
Boyapelly, Kumaraswamy
;
Alugubelli, Sathish Reddy
...
The Journal of Organic Chemistry. 76 (2011) 8 - p. 2568-2576 , 2011
Link:
https://doi.org/10.1021/..
?
6
The stereoselective total synthesis of (−)-achaetolide:
Thakur, Pallavi
;
Kumaraswamy, Boyapelly
;
Reddy, Gurram Raji
..
Tetrahedron: Asymmetry. 23 (2012) 8 - p. 547-553 , 2012
Link:
https://doi.org/10.1016/..
?
7
First stereoselective total synthesis of (−)-stagonolide A:
Srihari, Pabbaraja
;
Kumaraswamy, Boyapelly
;
Rao, Gokada Maheswara
.
Tetrahedron: Asymmetry. 21 (2010) 1 - p. 106-111 , 2010
Link:
https://doi.org/10.1016/..
?
8
Rationally Designed Pyrimidine Compounds: Promising Novel A..:
Guillaume Millette
;
Evelyne Lacasse
;
Renaud Binette
...
https://dx.doi.org/10.3390/antibiotics12081344. , 2023
Link:
https://doi.org/10.3390/..
?
9
Rationally Designed Pyrimidine Compounds: Promising Novel A..:
Guillaume Millette
;
Evelyne Lacasse
;
Renaud Binette
...
https://www.mdpi.com/2079-6382/12/8/1344. , 2023
Link:
https://doi.org/10.3390/..
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