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A modified Bischler-Napieralski procedure for the synthesis of 3-aryl-3,4-dihydroisoquinolines
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This article has been cited by 16 ACS Journal articles (5 most recent appear below).
Asymmetric Synthesis of (S)-(−)-Xylopinine. Use of the Sulfinyl Group as an Ipso Director in Aromatic SE
Virginia M. Mastranzo, Francisco Yuste, Benjamín Ortiz, Rubén Sánchez-Obregón, Rubén A. Toscano, and José L. García RuanoThe Journal of Organic Chemistry2011 Article ASAPAsymmetric Synthesis of (S)-(−)-Xylopinine. Use of the Sulfinyl Group as an Ipso Director in Aromatic SE
Virginia M. Mastranzo, Francisco Yuste, Benjamín Ortiz, Rubén Sánchez-Obregón, Rubén A. Toscano, and José L. García RuanoThe Journal of Organic Chemistry2011 Article ASAPOptically pure (S)-(−)-xylopinine 2 was prepared in three steps in 52% overall yield. Thus, condensation of the carbanion derived from (S)-4 with the (S)-(E)-sulfinylimine 5 gave a 2:1 mixture of tetrahydroisoquinolines 6a and 6b, differing only in ...
Synthesis of Gold Complexes Bearing Sterically Highly Encumbered, Chiral Carbene Ligands
Kristina Wilckens, Dieter Lentz, and Constantin CzekeliusOrganometallics2011 30 (6), 1287-1290Synthesis of Gold Complexes Bearing Sterically Highly Encumbered, Chiral Carbene Ligands
Kristina Wilckens, Dieter Lentz, and Constantin CzekeliusOrganometallics2011 30 (6), 1287-1290The synthesis of chiral carbene ligands derived from bis(tetrahydroisoquinoline) bearing sterically highly demanding, rigid substituents is described. Their corresponding gold complexes were structurally elucidated and successfully employed as catalysts ...
Enantioselective Total Synthesis and X-ray Structures of the Tetrahydroprotoberberine Alkaloids (−)-(S)-Tetrahydropalmatrubine and (−)-(S)-Corytenchine
Ahmed L. Zein, Louise N. Dawe and Paris E. GeorghiouJournal of Natural Products2010 73 (8), 1427-1430Enantioselective Total Synthesis and X-ray Structures of the Tetrahydroprotoberberine Alkaloids (−)-(S)-Tetrahydropalmatrubine and (−)-(S)-Corytenchine
Ahmed L. Zein, Louise N. Dawe and Paris E. GeorghiouJournal of Natural Products2010 73 (8), 1427-1430Enantioselective total syntheses and X-ray structures of both (S)-tetrahydropalmatrubine (2) and (S)-corytenchine (3) are reported for the first time. They were both derived from (S)-N-norlaudanidine, a benzyltetrahydroisoquinoline that was synthesized ...
A Versatile Cyclodehydration Reaction for the Synthesis of Isoquinoline and β-Carboline Derivatives
Mohammad Movassaghi and Matthew D. HillOrganic Letters2008 10 (16), 3485-3488A Versatile Cyclodehydration Reaction for the Synthesis of Isoquinoline and β-Carboline Derivatives
Mohammad Movassaghi and Matthew D. HillOrganic Letters2008 10 (16), 3485-3488The direct conversion of various amides to isoquinoline and β-carboline derivatives via mild electrophilic amide activation, with trifluoromethanesulfonic anhydride in the presence of 2-chloropyridine, is described. Low-temperature amide activation ...
Chiral N-Heterocyclic Carbenes with Restricted Flexibility in Asymmetric Catalysis
Denys Baskakov, Wolfgang A. Herrmann, Eberhardt Herdtweck, and Stephan D. HoffmannOrganometallics2007 26 (3), 626-632Chiral N-Heterocyclic Carbenes with Restricted Flexibility in Asymmetric Catalysis
Denys Baskakov, Wolfgang A. Herrmann, Eberhardt Herdtweck, and Stephan D. HoffmannOrganometallics2007 26 (3), 626-632A chiral C2-symmetric diamine was prepared from (S)-3-phenyl-3,4-dihydroisoquinoline by the virtue of asymmetric transformation. Rhodium and iridium complexes of chiral N-heterocyclic carbenes with restricted flexibility derived from 3,3‘-substituted ...
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- Published In Issue October, 1991
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