Zobrazeno 1 - 10
of 23
pro vyhledávání: '"S., Purushotham Reddy"'
Publikováno v:
In Chemico-Biological Interactions 1 August 2019 308:1-10
Publikováno v:
Russian Journal of General Chemistry. 88:774-779
An efficient, eco-friendly synthesis of a series of 2-{[3-oxo-3-(alkyl/aryl-1-yl)alkyl]thio}-3-substituted quinazolin-4(3H)-ones employing quinazolin-4(3H)-one and corresponding halo-acyl/haloalkyl as electrophiles is presented. The products were ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e99fc9ff63e9960eb77d88f149142daf
https://doi.org/10.1134/s1070363218040230
https://doi.org/10.1134/s1070363218040230
Publikováno v:
Chemico-biological interactions. 308
Diarylheptanoids display an array of biological and pharmacological properties. We previously reported the synthesis of a diarylheptanoid Alpinoid c and a series of its derivatives, evaluated their cytotoxicity against various human cancer cells. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf6560a616cdadc12c10a6152f0174ce
https://pubmed.ncbi.nlm.nih.gov/31071337
https://pubmed.ncbi.nlm.nih.gov/31071337
Publikováno v:
Synthetic Communications. 44:2886-2891
A highly convergent stereoselective total synthesis of stagonolide F is described starting from commercially available 5-hexen 1-ol using asymmetric dihydroxylation, Jacobsen's hydrolytic kinetic resolution (HKR), regioselective epoxide ring opening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f61c45496be520d11b0ca9db6ba23e43
https://doi.org/10.1080/00397911.2014.905602
https://doi.org/10.1080/00397911.2014.905602
Publikováno v:
Synthesis. 2012:311-315
Stereoselective concise total synthesis of leodomycin C and Dfrom commercially available propylene oxide using Jacobsen’s hydrolytickinetic resolution (HKR), base-promoted alkyne zipper reaction,TPP-promoted enyne ester (ynoate) to diene ester (die
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d23ec00d86e11b0d5a547d1f3dfec8e8
https://doi.org/10.1055/s-0031-1289640
https://doi.org/10.1055/s-0031-1289640
Publikováno v:
Synthesis. 2011:3180-3184
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f4b497fb6d2740f0d030d11326153d6
https://doi.org/10.1055/s-0030-1260183
https://doi.org/10.1055/s-0030-1260183
Autor:
T. Srikhanth Reddy, Yenamandra Venkateswarlu, S. Purushotham Reddy, V. Shekhar, D. Kumar Reddy
Publikováno v:
Tetrahedron: Asymmetry. 20:2315-2319
A simple and highly efficient stereoselective synthetic route has been developed for the synthesis of ( R )-rugulactone, a 6-arylalkyl-5,6-dihydro-2 H -pyran-2-one, from readily available substrates such as 1,3-propanediol and 3-phenyl-1-propanal emp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::251cb9aede1338e9e3c0d27893402944
https://doi.org/10.1016/j.tetasy.2009.09.016
https://doi.org/10.1016/j.tetasy.2009.09.016
Publikováno v:
ChemInform. 45
The first stereoselective synthesis of the title compound is presented using aminoxylation, Keck allylation, and a metathesis reaction as key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b0398f1eaa5b884c83041a7448d15df
https://doi.org/10.1002/chin.201442245
https://doi.org/10.1002/chin.201442245
Autor:
G.V.S. Bhanuprakash, V. Shekhar, Yenamandra Venkateswarlu, Baggu Chinnababu, J. Venkateswara Rao, L.R. Velatoor, D. Kumar Reddy, S. Purushotham Reddy
Publikováno v:
Bioorganicmedicinal chemistry letters. 22(12)
A simple, highly efficient and stereoselective synthetic route has been developed for synthesis of alpinoid-C ( 1 ) and its analogues ( 2 , 3 and 4 ) from commercially available starting materials by using Wittig olefination, Sharpless asymmetric epo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af9685ac731331f840dfcc67307bd0a8
https://pubmed.ncbi.nlm.nih.gov/22578452
https://pubmed.ncbi.nlm.nih.gov/22578452
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ba301953f388717ac9437f8c9e542a5
https://doi.org/10.1002/chin.199539164
https://doi.org/10.1002/chin.199539164