(Fluoren-9-ylmethoxy)carbonyl (Fmoc) amino acid chlorides. Synthesis, characterization, and application to the rapid synthesis of short peptide segments
- 1 September 1986
- journal article
- letter
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 51 (19) , 3732-3734
- https://doi.org/10.1021/jo00369a042
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- N-(Trifluoroacetyl)-.alpha.-amino acid chlorides as chiral reagents for Friedel-Crafts synthesisThe Journal of Organic Chemistry, 1985
- A simple method for synthesis of amides and peptides through acyl chloridesTetrahedron, 1985
- Friedel-Crafts acylation with N-(trifluoroacetyl)-.alpha.-amino acid chlorides. Application to the preparation of .beta.-arylalkylamines and 3-substituted 1,2,3,4-tetrahydroisoquinolinesThe Journal of Organic Chemistry, 1984
- Acid-stable, solvolytically deblocked amino-protecting-groups applications of the 1,3-dibromo-2-methyl-2-propyloxycarbonyl (DB-t-BOC) groupThe Journal of Organic Chemistry, 1984