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Convenient synthesis of benzyl ester
- Source :
- Bioorganic & Medicinal Chemistry Letters. 9:3119-3122
- Publication Year :
- 1999
- Publisher :
- Elsevier BV, 1999.
-
Abstract
- Mesylates or tosylates of delta-hydroxy-L-norvaline esters spontaneously afford L-proline esters upon exposure to aqueous buffer in near quantitative yield. This novel reaction has led to the development of a simple route to optically active proline esters.
- Subjects :
- Aqueous solution
Organic Chemistry
Clinical Biochemistry
Enantioselective synthesis
Pharmaceutical Science
Benzyl Compounds
Alkanesulfonates
Biochemistry
Chemical synthesis
chemistry.chemical_compound
Sulfonate
chemistry
Yield (chemistry)
Drug Discovery
Molecular Medicine
Organic chemistry
Proline
Molecular Biology
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 9
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi...........cdf8bdc85cda6d47be33b9856b5fc726
- Full Text :
- https://doi.org/10.1016/s0960-894x(99)00546-6