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November 3, 1997Helvetica Chimica Acta

Control of regio‐, diastereo‐, and enantioselectivity in the Ti(OTs)2(TADDOLato)‐catalyzed 1,3‐dipolar cycloaddition reaction between 3‐acryloyloxazolidin‐2‐one and nitrones

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Authors

KJKim B. JensenNovo Nordisk (Denmark)KGKurt V. GothelfAarhus UniversityKarl Anker JørgensenKarl Anker JørgensenUniversitat de València

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Jensen et al. (1997) studied this question.

synapsesocial.com/papers/6a962bea45c5500ab9bab91ehttps://doi.org/10.1002/hlca.19970800704
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1A Highly Diastereoselective and Enantioselective Ti(OTos)2−TADDOLate-Catalyzed 1,3-Dipolar Cycloaddition Reaction of Alkenes with Nitrones1996 · 134 citations
  2. 2On the Ti-TADDOLate-Catalyzed Diels-Alder Addition of 3-Butenoyl-1,3-oxazolidin-2-one to Cyclopentadiene. General Features of Ti-BINOLate- and Ti-TADDOLate-Mediated Reactions1995 · 150 citations
  3. 3Asymmetric Diels-Alder reaction catalyzed by a chiral titanium reagent1989 · 321 citations
  4. 4Preparation and Structural Analysis of Several New α,α,α′,α′‐Tetraaryl‐1,3‐dioxolane‐4,5‐dimethanols (TADDOL's) and TADDOL analogs, their evaluation as titanium ligands in the enantioselective addition of methyltitanium and diethylzinc reagents to benzaldehyde, and refinement of the mechanistic hypothesis1994 · 139 citations