Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Machender R. Madduru"'
Autor:
George A. Doss, Vinay V. Thakur, Gregori J. Morriello, Krishnan Malolanarasimhan, Spencer Knapp, Machender R. Madduru
Publikováno v:
Organic Letters. 8:1335-1337
[reaction: see text] Commercial 1,2:5,6-di-O-isopropylidene-alpha-d-allofuranose was converted to a protected bicyclic octosyl acid thioglycoside donor by a 10-step sequence that features an intramolecular ester enolate alkylation. Glycosylation of N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24c64f199ae64b5e92cfae062e6da845
https://doi.org/10.1021/ol0600382
https://doi.org/10.1021/ol0600382
Autor:
Zhijian Lu, Spencer Knapp, George A. Doss, Machender R. Madduru, Gregori J. Morriello, Thomas J. Emge
Publikováno v:
ChemInform. 33
Radical cyclization of 6 affords the bicyclic vinyl ether 9 with the appropriate stereochemistry for elaboration (seven steps) to griseolic acid B (1).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6a8d604db4fa36bfe41b731b1d30593
https://doi.org/10.1002/chin.200210201
https://doi.org/10.1002/chin.200210201
Autor:
Elisabeth Barofsky, Xiao-kun Zhang, Marcia I. Dawson, Machender R. Madduru, Max L. Deinzer, Mark Leid, Kai-Chia Feng, Valerie J. Peterson
Publikováno v:
The Biochemical journal. 362(Pt 1)
Apo and holo forms of retinoic acid receptors, and other nuclear receptors, display differential sensitivity to proteolytic digestion that likely reflects the distinct conformational states of the free and liganded forms of the receptor. We have deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bb0807504f048ffb5209d3a6dbacec5
https://pubmed.ncbi.nlm.nih.gov/11829754
https://pubmed.ncbi.nlm.nih.gov/11829754
Autor:
Thomas J. Emge, George A. Doss, Gregori J. Morriello, Zhijian Lu, Machender R. Madduru, Spencer Knapp
Publikováno v:
Organic letters. 3(22)
[reaction: see text]. Radical cyclization of 6 affords the bicyclic vinyl ether 9 with the appropriate stereochemistry for elaboration (seven steps) to griseolic acid B (1).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b721de206e6b549ea6b8b4ec4d1ff24
https://pubmed.ncbi.nlm.nih.gov/11678714
https://pubmed.ncbi.nlm.nih.gov/11678714