A method for the cleavage of t-butyl esters using silica gel in refluxing toluene is reported. Good yields of the corresponding carboxylic acids are obtained, and the reaction is selective for t-butyl esters over t-butyl ethers and trimethylsilylethyl (TMSE) esters.
β¦ LIBER β¦
Cinnamyl as a protecting group. A mild method for the cleavage of cinnamyl esters.
β Scribed by E.J. Corey; Marcus A. Tius
- Book ID
- 104235982
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- French
- Weight
- 111 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A mild and selective method for the clea
β
Randy W Jackson
π
Article
π
2001
π
Elsevier Science
π
French
β 89 KB
New protective groups for peptide synthe
β
D.S. Kemp; James Reczek
π
Article
π
1977
π
Elsevier Science
π
French
β 253 KB
As part of our long range program for developing a synthesis,' we wish to report the preparation and uses Maq esters. Esters of the 2-oxymethyleneanthraquinone tional operations of peptide synthesis but are cleaved mild reducing agents. compatible set of new reagents for peptide of a new carboxyl pr
A simple and mild method for the removal
β
Van der Eijk, Jan M.; Nolte, Roeland J. M.; Zwikker, Jan W.
π
Article
π
1980
π
American Chemical Society
π
English
β 291 KB
ChemInform Abstract: A Mild and Selectiv
β
Randy W. Jackson
π
Article
π
2010
π
John Wiley and Sons
β 30 KB
π 2 views
A new reagent for the cleavage of the te
β
A. Loffet; C. Dremier
π
Article
π
1971
π
Springer
π
English
β 512 KB
The methyl ester as a protective group:
β
Karsten SchΓΌrrle; Barbara Beier; Oleg Werbitzky; Wolfgang Piepersberg
π
Article
π
1991
π
Elsevier Science
π
English
β 347 KB