DOI: 10.1246/cl.1979.569. ASYMMETRIC SYNTHESIS OF 3-ALKYLSUCCINALDEHYDIC ACID METHYL ESTERS

ASYMMETRIC SYNTHESIS OF 3-ALKYLSUCCINALDEHYDIC ACID METHYL ESTERS

10.1246/cl.1979.569

Crossref journal-article

Oxford University Press (OUP)

Chemistry Letters (286)

Abstract

Abstract The highly stereoselective Michael addition was achieved by treating an aminal, prepared from (S)-2-(anilinomethyl)pyrrolidine and fumaraldehydic acid methyl ester, with the Grignard reagents. 3-Alkylsuccinaldehydic acid methyl esters were obtained with high enantiomeric excesses by the hydrolysis of the resulting aminals.

Bibliography

Asami, M., & Mukaiyama, T. (1979). ASYMMETRIC SYNTHESIS OF 3-ALKYLSUCCINALDEHYDIC ACID METHYL ESTERS. Chemistry Letters, 8(5), 569â572.

Authors 2

Masatoshi Asami (first)
Teruaki Mukaiyama (additional)

References 8 Referenced 34

10.1248/cpb.24.1273
10.1248/cpb.24.1288
10.1021/jo00399a021
10.1021/ja00439a071
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Dates

Type	When
Created	19 years, 1 month ago (July 24, 2006, 10:12 p.m.)
Deposited	1 year, 7 months ago (Jan. 19, 2024, 1:15 a.m.)
Indexed	1 year, 7 months ago (Jan. 19, 2024, 7:03 p.m.)
Issued	46 years, 3 months ago (May 1, 1979)
Published	46 years, 3 months ago (May 1, 1979)
Published Online	19 years, 5 months ago (March 27, 2006)
Published Print	46 years, 3 months ago (May 5, 1979)

Funders 0

None

BibTeX

@article{Asami_1979, title={ASYMMETRIC SYNTHESIS OF 3-ALKYLSUCCINALDEHYDIC ACID METHYL ESTERS}, volume={8}, ISSN={1348-0715}, url={http://dx.doi.org/10.1246/cl.1979.569}, DOI={10.1246/cl.1979.569}, number={5}, journal={Chemistry Letters}, publisher={Oxford University Press (OUP)}, author={Asami, Masatoshi and Mukaiyama, Teruaki}, year={1979}, month=may, pages={569–572} }

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