Zum stereochemischen Verlauf der Biosynthese von 2‐Oxo‐pantolacton: Synthese von stereospezifisch indiziertem Pantolacton aus Äpfelsäure
- 3 February 1982
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 65 (1) , 344-352
- https://doi.org/10.1002/hlca.19820650136
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- 2, 3‐Disubstituted γ‐Butyrolactams from the Michael‐Additions of Doubly Deprotonated, Optically Active β‐Hydroxycarboxylates to Nitroolefins. Preliminary CommunicationHelvetica Chimica Acta, 1980
- Chiral Reagents from Tartaric Acid—1‐Benzyloxy‐3,4‐epoxy‐2‐butanol, a Versatile Intermediate for the Synthesis of EnantiomersAngewandte Chemie International Edition in English, 1979
- Über die Stereospezifität der α‐Alkylierung von β‐Hydroxycarbonsäureestern. Vorläufige MitteilungHelvetica Chimica Acta, 1979
- Effective biomimetic route to D-(+)-pantothenate using asymmetric hydrogenation catalyzed by a chiral rhodium complex in the key stepThe Journal of Organic Chemistry, 1978
- A convenient method for estimation of alkyllithium concentrationsThe Journal of Organic Chemistry, 1976
- The Preparation of Four Optically Active Isomers of 3-Methylmalic AcidBulletin of the Chemical Society of Japan, 1966
- A Novel Resolution of Pantolactone—The Synthesis of D(+)-Calcium Pantothenate1Journal of the American Chemical Society, 1957
- α-Hydroxy-β,β-dimethyl-γ-butyrolactoneJournal of the American Chemical Society, 1941
- Pantothenic Acid. VIII. The Total Synthesis of Pure Pantothenic AcidJournal of the American Chemical Society, 1940
- Polyoxy‐acyl‐derivate des β‐AlaninsHelvetica Chimica Acta, 1940