.alpha.-Amino acid derivatives as chiral educts for asymmetric products. Synthesis of sphingosine from .alpha.'-amino-.alpha.,.beta.-ynones
- 1 December 1986
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 51 (26) , 5320-5327
- https://doi.org/10.1021/jo00376a050
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Enantioselective Synthesis of D‐erythro‐Sphingosine and of CeramideHelvetica Chimica Acta, 1986
- .alpha.-Amino acids as chiral educts for asymmetric products. The synthesis of .alpha.'-amino-.alpha.,.beta.-ynonesThe Journal of Organic Chemistry, 1985
- .alpha.-Amino acids as chiral educts for asymmetric products. Chirospecific syntheses of methyl L-sibirosaminide and its C-3 epimer from L-allothreonineThe Journal of Organic Chemistry, 1985
- .alpha.-Amino acids as chiral educts for asymmetric products. A general synthesis of D-.alpha.-amino acids from L-serineJournal of the American Chemical Society, 1984
- Synthesis of (3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid derivatives. Analysis of diastereomeric purityThe Journal of Organic Chemistry, 1978