Search Results - "Houser, Jeffrey H."
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Tandem Asymmetric Cyclopropanation/Cope Rearrangement. A Highly Diastereoselective and Enantioselective Method for the Construction of 1,4-Cycloheptadienes
Published in Journal of the American Chemical Society (15-04-1998)“…Decomposition of vinyldiazoacetates by rhodium(II) (N-dodecylbenzenesulfonyl)prolinate (Rh2(S-DOSP)4, 1) in the presence of dienes results in a direct and…”
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Modular Mo-based catalysts for efficient asymmetric olefin metathesis. Catalytic enantioselective synthesis of cyclic ethers and acetals
Published in Tetrahedron letters (02-12-2000)“…Chiral Mo-based complexes 1– 3 promote the catalytic enantioselective ring-closing metathesis of various polyenes to afford unsaturated furans, pyrans and…”
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Enantioselective Synthesis of Functionalized Tropanes by Rhodium(II) Carboxylate-Catalyzed Decomposition of Vinyldiazomethanes in the Presence of Pyrroles
Published in Journal of organic chemistry (21-02-1997)“…A series of enantiomerically enriched tropanes was synthesized by the rhodium(II) octanoate-catalyzed reaction of various N-BOC-protected pyrroles with…”
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A Readily Available and User-Friendly Chiral Catalyst for Efficient Enantioselective Olefin Metathesis
Published in Angewandte Chemie International Edition (17-04-2001)“…No glove box required! A new chiral catalyst for olefin metathesis is prepared from commercially available materials and is equally or more effective and…”
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Synthesis of Molybdenum Imido Alkylidene Complexes That Contain 3,3‘-Dialkyl-5,5‘,6,6‘-tetramethyl-1,1‘-biphenyl-2,2‘-diolates (Alkyl = t-Bu, Adamantyl). Catalysts for Enantioselective Olefin Metathesis Reactions
Published in Organometallics (04-09-2000)“…Two 3,3‘-dialkyl-5,5‘,6,6‘-tetramethyl-1,1‘-biphenyl-2,2‘-diols (where alkyl = t-Bu, adamantyl) were prepared in two steps and resolved as the menthol…”
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Synthesis and Chemistry of Donor/Acceptor-Substituted Cyclopropenes
Published in Journal of organic chemistry (01-11-1995)Get full text
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A Readily Available and User-Friendly Chiral Catalyst for Efficient Enantioselective Olefin Metathesis This research was supported by the National Institutes of Health (GM-59426) and the National Science Foundation (CHE-9905806 to A. H. H. and CHE-9988766 to R. R. S.)
Published in Angewandte Chemie International Edition (17-04-2001)Get full text
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A Readily Available and User-Friendly Chiral Catalyst for Efficient Enantioselective Olefin Metathesis
Published in Angewandte Chemie (17-04-2001)“…Hier braucht man keine Handschuhbox mehr! Aus kommerziell erhältlichen Ausgangsverbindungen kann ein neuer Katalysator für die Olefin‐Metathese hergestellt…”
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A Readily Available and User-Friendly Chiral Catalyst for Efficient Enantioselective Olefin Metathesis
Published in Angewandte Chemie (17-04-2001)Get full text
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