102794-92-3Relevant articles and documents
An enantiocontrolled synthesis of pyrrolizidines, (-)-platynecine and (-)-hadinecine
Kang, Sung Ho,Kim, Geun Tae,Yoo, Yong Sang
, p. 603 - 606 (1997)
Trisubstituted allylic alcohols 13 and 14 have been converted into a single isomeric trans-oxazoline 16 via an intramolecular iodoamidation of the corresponding trichloroacetimidates, which have been elaborated into (-)-platynecine 1 and(-)-hadinecine 2 via a common intermediate pyrrolizidine.
Stereoselective, Ag-Catalyzed Cyclizations to Access Polysubstituted Pyran Ring Systems: Synthesis of C1-C12 Subunit of Madeirolide A
Watanabe, Kazuhiro,Li, Jinming,Veerasamy, Nagarathanam,Ghosh, Ankan,Carter, Rich G.
supporting information, p. 1744 - 1747 (2016/05/19)
The exploration into the scope of a silver-catalyzed cyclization (AgCC) of propargyl benzoates for accessing pyran ring systems has been reported. The impact of the degree of substitution, nature of the substitution on the carbon backbone/benzoate moiety,
ANTIBACTERIAL AGENTS
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Page/Page column 132, (2013/12/03)
Antibacterial compounds of formula (I) are provided, as well as stereoisomers and pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising such compounds; methods of treating bacterial infections by the administration of such compounds; and processes for the preparation of such compounds.