Zobrazeno 1 - 10
of 10
pro vyhledávání: '"B. Phaneendra Reddy"'
Publikováno v:
Synlett. 25:501-504
A stereoselective total synthesis of phomolides G and H, a polyketide natural products is described. The synthesis involves organocatalytic enantioselective asymmetric epoxidation, C1-Wittig olefination, and ring-closing metathesis as key steps. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5de8717077baec007da46c7a9c0c4071
https://doi.org/10.1055/s-0033-1340348
https://doi.org/10.1055/s-0033-1340348
Publikováno v:
Tetrahedron Letters. 54:5781-5784
A concise approach for the total synthesis of attenols A and B is described involving MacMillan’s α-aminooxylation, Evan’s asymmetric alkylation, Brown’s allylation, and spiro-ketalization as key steps. This approach has successfully demonstra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a402ed6efc19f3bec105cf3c8d6a321
https://doi.org/10.1016/j.tetlet.2013.08.043
https://doi.org/10.1016/j.tetlet.2013.08.043
Publikováno v:
Tetrahedron Letters. 53:5749-5752
A highly stereoselective approach to the total synthesis of seimatopolide A and (2 S ,3 R ,5 S )-(−)-2,3-dihydroxytetradecan-5-olide is described via a common polyketide precursor by means of Prins reaction and MacMillan aminoxylation sequence.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64bdf412fb00558d3b350b92cd2c80c4
https://doi.org/10.1016/j.tetlet.2012.08.027
https://doi.org/10.1016/j.tetlet.2012.08.027
Autor:
P. Sivaramakrishna Reddy, J. S. Yadav, Ahamad Al Khazim Al Ghamdi, B. Phaneendra Reddy, B. V. Subba Reddy
Publikováno v:
Tetrahedron Letters. 54:5758-5760
A stereoselective total synthesis of xyolide is described employing MacMillan α-hydroxylation, Steglich esterification, and ring closing metathesis as key steps. The use of organocatalytic MacMillan α-hydroxylation to construct two of the chiral ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cc3f3b2a977c5eab8c0d3d81b6774a5
https://doi.org/10.1016/j.tetlet.2013.08.038
https://doi.org/10.1016/j.tetlet.2013.08.038
Autor:
P. Sivaramakrishna Reddy, B. V. Subba Reddy, J. S. Yadav, Y. Jayasudhan Reddy, B. Phaneendra Reddy
Publikováno v:
Tetrahedron Letters. 54:4960-4962
A novel and efficient approach has been developed for the total synthesis of (+)-8-ethylnorlobelol ( 1 ) in a highly stereoselective manner. The key anti -1,3-aminoalcohol core is constructed through the reductive opening of 2-iodomethyl-4-amidotetra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fafd99e10c392e37b05a5bd7d642f15
https://doi.org/10.1016/j.tetlet.2013.07.026
https://doi.org/10.1016/j.tetlet.2013.07.026
Publikováno v:
Tetrahedron Letters. 52:2306-2308
The stereoselective total synthesis of (−)-cleistenolide is described employing the Barbier allylation, MacMillan α-hydroxylation, Stille–Gennari olefination, and CeCl3·7H2O mediated lactonization as key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::458a91ceb6c51fa73c2eab692d7abdfa
https://doi.org/10.1016/j.tetlet.2011.02.025
https://doi.org/10.1016/j.tetlet.2011.02.025
Publikováno v:
ChemInform. 45
Phomolides G (Ia) and H (Ib) are prepared in 15 and 17 steps with 18% and 16% overall yields, resp., involving MacMillan asymmetric epoxydation, Steglich esterification and ring closing metathesis as the key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40b22ec2e7ae4503f62d9d5649a1fc1e
https://doi.org/10.1002/chin.201433232
https://doi.org/10.1002/chin.201433232
Autor:
Ahamad Al Khazim Al Ghamdi, B. Phaneendra Reddy, B. V. Subba Reddy, J. S. Yadav, P. Sivaramakrishna Reddy
Publikováno v:
ChemInform. 45
A stereoselective total synthesis of xyolide (I) is described employing MacMillan α-hydroxylation, Steglich esterification, and ring closing metathesis as key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e086cdffe0d14f1dfabd98d7b28936c8
https://doi.org/10.1002/chin.201406204
https://doi.org/10.1002/chin.201406204
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Akademický článek
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