Simple and efficient cleavage reaction of the boc group in heterocyclic compounds
- 1 January 2004
- journal article
- research article
- Published by Wiley in Journal of Heterocyclic Chemistry
- Vol. 41 (1), 57-60
- https://doi.org/10.1002/jhet.5570410109
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- General synthesis of n-membered cyclic sulfamidesTetrahedron, 2003
- Synthese et N-Acylation Regiospecifique de 1,2,5-Thiadiazolidines 1,1-Dioxydes ChiralesPhosphorus, Sulfur, and Silicon and the Related Elements, 2003
- Synthesis of 1,2,5-Thiadiazolidines 1,1-dioxides (Cyclosulfamides) Starting from Amino Acids and Chlorosulfonyl IsocyanateTetrahedron, 2000
- Photocyclization strategy for the synthesis of antitumor agent CC-1065: synthesis of dideoxy PDE-I and PDE-II. Synthesis of thiophene and furan analogs of dideoxy PDE-I and PDE-IIThe Journal of Organic Chemistry, 1987
- Use of 10% sulfuric acid/dioxane for removal of N‐α‐tertiary‐butyloxycarbonyl group during solid phase peptide synthesisInternational Journal of Peptide and Protein Research, 1986
- Selective transformation of N-Tetrahedron Letters, 1985
- The Modification of Tryptophyl Residues during the Acidolytic Cleavage of Boc-groups. I. Studies with Boc-TryptophanBulletin of the Chemical Society of Japan, 1980
- REMOVAL OF t‐BUTYL AND t‐BUTOXYCARBONYL PROTECTING GROUPS WITH TRIFLUOROACETIC ACIDInternational Journal of Peptide and Protein Research, 1978