A Conformational Model for MTPA Esters of Chiral N-(2-Hydroxyalkyl)‎acrylamides

Joint Authors

Rustoy, Eduardo M.
Baldessari, Alicia
Monsalve, Leandro N.

Source

Advances in Chemistry

Issue

Vol. 2014, Issue 2014 (31 Dec. 2014), pp.1-6, 6 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2014-08-10

Country of Publication

Egypt

No. of Pages

6

Main Subjects

Chemistry

Abstract EN

The absolute stereochemistry of novel chiral N-(2-hydroxylalkyl)acrylamides prepared by a lipase-catalyzed resolution was successfully determined by 1H NMR of their MTPA esters.

The method was validated for this particular case by computational experiments.

American Psychological Association (APA)

Rustoy, Eduardo M.& Baldessari, Alicia& Monsalve, Leandro N.. 2014. A Conformational Model for MTPA Esters of Chiral N-(2-Hydroxyalkyl)acrylamides. Advances in Chemistry،Vol. 2014, no. 2014, pp.1-6.
https://search.emarefa.net/detail/BIM-494599

Modern Language Association (MLA)

Rustoy, Eduardo M.…[et al.]. A Conformational Model for MTPA Esters of Chiral N-(2-Hydroxyalkyl)acrylamides. Advances in Chemistry No. 2014 (2014), pp.1-6.
https://search.emarefa.net/detail/BIM-494599

American Medical Association (AMA)

Rustoy, Eduardo M.& Baldessari, Alicia& Monsalve, Leandro N.. A Conformational Model for MTPA Esters of Chiral N-(2-Hydroxyalkyl)acrylamides. Advances in Chemistry. 2014. Vol. 2014, no. 2014, pp.1-6.
https://search.emarefa.net/detail/BIM-494599

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-494599