PREPARATION OF OPTICALLY ACTIVE NEW MERCAPTO CHIRAL AUXILIARIES DERIVED FROM CAMPHOR
- 1 December 1993
- journal article
- research article
- Published by Taylor & Francis in Organic Preparations and Procedures International
- Vol. 25 (6) , 673-679
- https://doi.org/10.1080/00304949309356263
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Stereoselective addition reactions of chiral N-benzylidene-p-toluenesulfinamides. Asymmetric syntheses of .beta.- and .gamma.-amino acidsThe Journal of Organic Chemistry, 1991
- (-)-.alpha.,.alpha.-Dichlorocamphorsulfonyloxaziridine: a superior reagent for the asymmetric oxidation of sulfides to sulfoxidesJournal of the American Chemical Society, 1989
- Preparation of stable, camphor-derived, optically active allyl and alkyl sulfoxides and thermal epimerization of the allyl sulfoxidesThe Journal of Organic Chemistry, 1988
- Asymmetric oxidation of sulfides mediated by chiral titanium complexes : mechanistic and synthetic aspectsTetrahedron, 1987
- Camphor derivatives as chiral auxiliaries in asymmetric synthesisTetrahedron, 1987
- Aymmetric synthesis of () - and ()-citramalate in high enantiomeric purityTetrahedron Letters, 1985
- Studies on the preparation and reactions of tritylsulfeniminesThe Journal of Organic Chemistry, 1983
- Functional Groups at Concave Sites: Asymmetric Diels‐Alder Synthesis with Almost Complete (Lewis‐Acid Catalyzed) or High (Uncatalyzed) StereoselectivityAngewandte Chemie International Edition in English, 1981
- Asymmetric Synthesis Using Nucleophilic Reagents Containing a Chiral Sulfoxide GroupSynthesis, 1981
- Synthesis of a cephalosporin analogueJournal of the Chemical Society, Perkin Transactions 1, 1977