Generation of chiral olefins based on L-aspartic acid

Schlachter I, Fröhlich R, Mattay J (1997)
Journal für praktische Chemie 339(1): 66-70.

Journal Article | Published | English

No fulltext has been uploaded

Author
; ;
Abstract
A new chiral olefin 4 was synthesized starting from L-aspartic acid. The structures of the intermediate oxazolidinones 6 and 7 were proven by X-ray analysis to be diastereomers. it was shown that 4 is unreactive in Diels-Alder reactions with cyclopentadiene and 1,3-diphenylisobenzofuran because of its steric overloading (M.M. calculations) rather than by electronic effects (FMO by AM1 calculations).
Publishing Year
ISSN
eISSN
PUB-ID

Cite this

Schlachter I, Fröhlich R, Mattay J. Generation of chiral olefins based on L-aspartic acid. Journal für praktische Chemie. 1997;339(1):66-70.
Schlachter, I., Fröhlich, R., & Mattay, J. (1997). Generation of chiral olefins based on L-aspartic acid. Journal für praktische Chemie, 339(1), 66-70.
Schlachter, I., Fröhlich, R., and Mattay, J. (1997). Generation of chiral olefins based on L-aspartic acid. Journal für praktische Chemie 339, 66-70.
Schlachter, I., Fröhlich, R., & Mattay, J., 1997. Generation of chiral olefins based on L-aspartic acid. Journal für praktische Chemie, 339(1), p 66-70.
I. Schlachter, R. Fröhlich, and J. Mattay, “Generation of chiral olefins based on L-aspartic acid”, Journal für praktische Chemie, vol. 339, 1997, pp. 66-70.
Schlachter, I., Fröhlich, R., Mattay, J.: Generation of chiral olefins based on L-aspartic acid. Journal für praktische Chemie. 339, 66-70 (1997).
Schlachter, I, Fröhlich, R, and Mattay, Jochen. “Generation of chiral olefins based on L-aspartic acid”. Journal für praktische Chemie 339.1 (1997): 66-70.
This data publication is cited in the following publications:
This publication cites the following data publications:

Export

0 Marked Publications

Open Data PUB

Web of Science

View record in Web of Science®

Search this title in

Google Scholar