Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Lisa M. Reeder"'
Autor:
Gino Gabellone, Lloyd Charles Franklin, Thomas Norman Nanninga, Lisa M. Reeder, Niamh J. Panesar, Kyle Kissick, Catherine Dunne, Stuart Field, Martinez Carlos, John W. Wong, George Smith, James Saenz, Margaret Claire Evans, Lorraine Murtagh, John G. Van Alsten
Publikováno v:
Organic Process Research & Development. 15:1315-1327
Three synthetic approaches, suitable for the large scale manufacture of the α2δ-ligand, (3S,5R)-3-(aminomethyl)-5-methyloctanoic acid 3, have been evaluated. The selected seven step manufacturing process has then been optimized and used to deliver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40f4690618c9c38799606815eec00d7c
https://doi.org/10.1021/op2001832
https://doi.org/10.1021/op2001832
Publikováno v:
Organic Process Research & Development. 12:989-994
Perchloric acid appears unique in its ability to catalyze stereoselective trans-acetalizations of steroids. However, the requisite recipes result in an intermediate phase enriched in perchlorate and organic material with the potential for catastrophi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8dabd89227182cf30b7b3513d3bee48
https://doi.org/10.1021/op800128g
https://doi.org/10.1021/op800128g
Autor:
Robert K. Boeckman, Lisa M. Reeder
Publikováno v:
Synlett. :1399-1403
Based upon X-ray structural information derived from a series of camphor-derived bicyclic lactam chiral controller molecules, a new auxiliary has been designed which affords superior diastereoselectivity (>95:5) in Diels-Alder reactions with common d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4810e2db7dbe4dfc2252f1dd5d1f8366
https://doi.org/10.1055/s-2004-829091
https://doi.org/10.1055/s-2004-829091
Autor:
Lisa M. Reeder, Louis S. Hegedus
Publikováno v:
The Journal of Organic Chemistry. 64:3306-3311
The ring expansion of 22 differently beta-substituted alpha-methyl-alpha-methoxycyclobutanones by diazomethane was studied. Migration of the less-substituted alpha-carbon was favored with the single exception of a very sterically hindered beta-benzyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fdf034fee70e807c455505e889b105a
https://doi.org/10.1021/jo990226o
https://doi.org/10.1021/jo990226o
Autor:
Lisa M. Reeder, Louis S. Hegedus
Publikováno v:
ChemInform. 30
The ring expansion of 22 differently β-substituted α-methyl-α-methoxycyclobutanones by diazomethane was studied. Migration of the less-substituted α-carbon was favored with the single exception of a very sterically hindered β-benzyloxy β-substi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1cf408915b8670513343abeb3c1a4f1
https://doi.org/10.1002/chin.199937077
https://doi.org/10.1002/chin.199937077
Autor:
Lorraine Murtagh, Catherine Dunne, Gino Gabellone, Niamh J. Panesar, Stuart Field, Lisa M. Reeder, James Saenz, George P. Smith, Kyle Kissick, Carlos, Martinez, John G. Van Alsten, Margaret C. Evans, Lloyd C. Franklin, Thomas Nanninga, John Wong
Publikováno v:
Organic Process Research & Development; Nov2011, Vol. 15 Issue 6, p1315-1327, 13p
Publikováno v:
Organic Process Research & Development; Aug2008, Vol. 12 Issue 5, p989-994, 6p