Reactions of a new optically active arylperhydronaphthalenol based chiral auxiliary
- 1 December 1992
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 3 (12) , 1533-1536
- https://doi.org/10.1016/s0957-4166(00)86053-x
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Diastereoselective reduction of an α-keto-ester derived from (−)-8-phenylmenthol: A 4-step synthesis of R-Halostachine analogue.Tetrahedron: Asymmetry, 1991
- Configuration and conformation of (−)-8-phenylmenthyl 3-amino-2-hydroxy-5-methylhexanoateTetrahedron, 1991
- Auxiliary structure and asymmetric induction in the ene reactions of chiral glyoxylatesThe Journal of Organic Chemistry, 1986
- Preparation of 8-phenylmenthol and its diastereomer, 2-epi,ent-8-phenylmenthol. A caveatThe Journal of Organic Chemistry, 1986
- Photophysical probes of intramolecular interactions responsible for asymmetric inductionThe Journal of Organic Chemistry, 1985
- High asymmetric induction in diels-alder additions of cyclopentadiene to acrylates derived from isoborneolTetrahedron Letters, 1982
- Asymmetric induction in Diels‐Alder reactions to acrylates derived from chiral sec‐alcohols. Preliminary communicationHelvetica Chimica Acta, 1981
- Resolution, Stereochemial Correlation and Maximum Rotations of the Norbornane- and 5-Norbornene-2-carboxylic Acids. Isotope Dilution as an Aid in the Determination of Optical Purity1Journal of the American Chemical Society, 1959