64028-90-6Relevant articles and documents
Inter-and intramolecular annulation strategies to a cyclopentanone building block containing an all-carbon quaternary stereogenic center
Penrose, Stephen D.,Stott, Andrew J.,Breccia, Perla,Haughan, Alan F.,Bürli, Roland W.,Jarvis, Rebecca E.,Dominguez, Celia
supporting information, p. 1401 - 1404 (2015/03/30)
Synthesis of (S)-2-methyl-3-fluorophenyl cyclopentanone methyl ester (1S)-1 has been achieved by both inter-and intramolecular alkylation reactions on multigram scale, using chiral pool reagents. The intramolecular variant is a novel example of a chiral bis-electrophile reacting with a carbon nucleophile to form an enantiomerically pure all-carbon quaternary center.
HISTONE DEACETYLASE INHIBITORS AND COMPOSITIONS
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Paragraph 00149, (2014/10/15)
Provided are certain histone deacetylase (HDAC) inhibitors of Formula (I), compositions thereof, and methods of their use.
Synthesis of optically active 2-methyl- and 2-ethyl-1,6-dioxaspiro[4.4]nonane- and -[4.5]decane pheromones from a common chiral precursor
Hungerbuhler,Naef,Wasmuth,et al.
, p. 1960 - 1970 (2007/10/02)
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