Synthesis of both enantiomers of C2 symmetric trans-2,5-bis(hydroxymethyl)pyrrolidine. Lipase mediated sequential kinetic resolutions
- 11 July 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (28) , 4915-4918
- https://doi.org/10.1016/s0040-4039(00)73281-3
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Enantioselective iodolactonization through diastereotopic group differentiationTetrahedron Letters, 1990
- C2 symmetry and asymmetric inductionChemical Reviews, 1989
- Diastereoselective Reduction of α-Keto Amides Having trans-2,5-Disubstituted Pyrrolidine as a Chiral AuxiliaryBulletin of the Chemical Society of Japan, 1989
- Control of the stereoselectivity of pig liver esterase by different reaction conditions in the hydrolysis of cis-N-benzyl-2,5-bismethoxycarbonylpyrrolidine and structurally related diestersBioorganic Chemistry, 1988
- Asymmetric Diels–Alder Reaction of Acrylamides Having trans-2,5-Disubstituted Pyrrolidines as Chiral AuxiliariesBulletin of the Chemical Society of Japan, 1987
- Diastereoselective Reduction of α-Keto Amides Having trans-2,5-Disubstituted Pyrrolidines as Chiral AuxiliariesChemistry Letters, 1987
- Asymmetric reactions using C2-symmetrically 2,5-disubstituted pyrrolidines as chiral auxiliaries.Journal of Synthetic Organic Chemistry, Japan, 1986
- Asymmetric aldol reaction of amide enolates bearing -2,5-disubstituted pyrrolidines as chiral auxiliariesTetrahedron Letters, 1985
- A highly effective asymmetric synthesis of α-hydroxy acids by alkylation of chiral -(benzyloxyacetyl)--2,5-bis(methoxymethoxymethyl)pyrrolidineTetrahedron Letters, 1985
- Asymmetric alkylation of carboxyamides by using trans-2,5-disubstituted pyrrolidines as chiral auxiliariesTetrahedron Letters, 1984