Intramolecular Pictet-Spengler reaction of N-alkoxytryptamines. 3. Stereoselective synthesis of (-)-debromoeudistomin L and (-)-O-methyldebromoeudistomin E and their stereoisomers
- 1 June 1990
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 55 (13) , 3998-4006
- https://doi.org/10.1021/jo00300a011
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Intramolecular Pictet-Spengler reaction of N-alkoxytryptophans and tryptamines. 2. Synthesis of Corynanthe alkaloid derivatives containing a tetrahydro-1,2-oxazine as the D ringThe Journal of Organic Chemistry, 1990
- Eudistomins From the New Zealand Ascidian Ritterella sigillinoidesAustralian Journal of Chemistry, 1989
- Eudistomins A-Q, .beta.-carbolines from the antiviral Caribbean tunicate Eudistoma olivaceumJournal of the American Chemical Society, 1987
- Synthesis of 2-hydroxy-3-(ethoxycarbonyl)-1,2,3,4-tetrahydro-.beta.-carbolines from N-hydroxytryptophans. An approach to the eudistomin seriesThe Journal of Organic Chemistry, 1987
- Synthesis of (racemization prone) optically active thiols by SN2 substitution using cesium thiocarboxylatesThe Journal of Organic Chemistry, 1986
- Total synthesis of the antibiotic sparsomycin, a modified uracil amino acid monoxodithioacetalThe Journal of Organic Chemistry, 1981
- REMOVAL OF t‐BUTYL AND t‐BUTOXYCARBONYL PROTECTING GROUPS WITH TRIFLUOROACETIC ACIDInternational Journal of Peptide and Protein Research, 1978