专利号:US-7119232-B2 优先权日:2004-03-26 标题 :Nucleophilic substitution reactions of difluorormethyl phenyl sulfone with alkyl halides leading to the facile synthesis of terminal 1,1-difluoro-1-alkenes and difluoromethylalkanes 发明人:PRAKASH G K SURYA; HU JINBO; OLAH GEORGE A; WANG YING 权利人:UNIV SOUTHERN CALIFORNIA 摘要:(Benzenesulfonyl)difluoromethyl anion, in situ generated from difluoromethyl phenyl sulfone and a base, was found to easily undergo nucleophilic substitution reactions (S N 2) with primary alkyl halides, elemental halogens, and perfluoroalkyl halides with good selectivity. The formed (benzenesufonyl)difluoromethylalkanes are useful intermediates for the facile preparation of 1,1-difluoro-1-alkenes and difluoromethylalkanes. Thus, difluoromethyl phenyl sulfone acts as both “CF 2 â•?â€? and “CF 2 H − â€? synthons
专利号:US-12129274-B2 优先权日:2018-04-03 标题:Modular synthesis of aminoglycosides 发明人:CALABRESE ANDREW ANTONY; KANE TIMOTHY ROBERT; HILDEBRANDT DARIN; LOPEZ MICHAEL; EVDOKIMOV NIKOLAI; COHEN FREDERICK; BAYRAKDARIAN MALKEN; XU SANIJIA; DESJARDINS SAMUEL; SOUEIDAN OLIVIER 权利人:REVAGENIX INC 摘要:The present disclosure relates to novel methods for preparing antibacterial aminoglycoside compounds and the compounds used in such preparations.
专利号:US-2022411456-A1 优先权日:2018-04-03 标题 :Modular synthesis of aminoglycosides
专利号:US-11673907-B2 优先权日:2018-04-03 标 题:Modular synthesis of aminoglycosides
专利号:US-2006052643-A1 优先权日:2004-03-26 标题:Nucleophilic substitution reactions of difluorormethyl phenyl sulfone with alkyl halides leading to the facile synthesis of terminal 1,1-difluoro-1-alkenes and difluoromethylalkanes
专利号:US-9029563-B2 优先权日:2012-01-06 标题:Substituted 1-benzylindolin-2-one analogs as positive allosteric modulators of muscarinic acetylcholine M1 receptors 发明人:LINDSLEY CRAIG W; CONN P JEFFREY; WOOD MICHAEL R; MELANCON BRUCE J; POSLUSNEY MICHAEL S 权利人:UNIV VANDERBILT 摘要:In one aspect, the invention relates to substituted 1-benzylindolin-2-one analog compounds, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the muscarinic acetylcholine receptor M 1 (mAChR M 1 ); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.