Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ahamad Al Khazim Al Ghamdi"'
Publikováno v:
Tetrahedron Letters. 52:6709-6712
A stereoselective synthesis of fragment A of cryptophycin is achieved utilizing the versatile Prins cyclization. Subsequently, the total synthesis of cryptophycin-24 (arenastatin A) has been accomplished by coupling it with the depsipeptide subunit.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca18f764cd228bc95d3f7e7590de10d9
https://doi.org/10.1016/j.tetlet.2011.09.134
https://doi.org/10.1016/j.tetlet.2011.09.134
Autor:
Ragam Nageshwar Rao, Basi V. Subba Reddy, K. Ravindar, Jhillu S. Yadav, Begari Prem Kumar, Ahamad Al Khazim Al Ghamdi, R. Somaiah
Publikováno v:
Synthesis. 2011:3168-3172
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1741c943faa6d421c4bbb67a6c6052ee
https://doi.org/10.1055/s-0030-1260190
https://doi.org/10.1055/s-0030-1260190
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
Publikováno v:
Tetrahedron Letters. 52:2943-2945
An expedient stereoselective total synthesis of 18-carbon (+)-(6 S ,9 R ,10 R )-bovidic acid, isolated from the pelage and skin of a gaur B. frontalis is described using l -proline catalysed sequential α-aminoxylation and Horner–Wadsworth–Emmons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b816c72341d1d25bf79e40f29bd00b0c
https://doi.org/10.1016/j.tetlet.2011.03.089
https://doi.org/10.1016/j.tetlet.2011.03.089
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
Publikováno v:
Carbohydrate research. 358
Total synthesis of (−)-(5R,6S)-6-acetoxy-5-hexadecanolide, a major component of mosquito oviposition attractant pheromones is reported. The key synthetic steps involve epoxide opening by lithiated salt of ethylpropionate and acid catalysed lactoniz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfbecb97174e22a35440d4f83d92d382
https://pubmed.ncbi.nlm.nih.gov/22687338
https://pubmed.ncbi.nlm.nih.gov/22687338