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2-tert-butyl-3-methyl-2,3-dihydroimidazol- 4-one-N-oxide: a new nitrone-based chiral glycine equivalent.

Publication ,  Journal Article
Baldwin, SW; Long, A
Published in: Organic letters
May 2004

Cycloaddition reactions between a new homochiral imidazolone-derived nitrone afford cycloadducts in high yield and with high stereoselectivity. Subsequent cycloadduct elaboration affords the gamma-lactones of gamma-hydroxy-alpha-amino acids as well as the optically pure amino acids themselves.

Duke Scholars

Published In

Organic letters

DOI

EISSN

1523-7052

ISSN

1523-7060

Publication Date

May 2004

Volume

6

Issue

10

Start / End Page

1653 / 1656

Related Subject Headings

  • Organic Chemistry
  • 34 Chemical sciences
  • 03 Chemical Sciences
 

Citation

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Baldwin, S. W., & Long, A. (2004). 2-tert-butyl-3-methyl-2,3-dihydroimidazol- 4-one-N-oxide: a new nitrone-based chiral glycine equivalent. Organic Letters, 6(10), 1653–1656. https://doi.org/10.1021/ol049505a
Baldwin, Steven W., and Alan Long. “2-tert-butyl-3-methyl-2,3-dihydroimidazol- 4-one-N-oxide: a new nitrone-based chiral glycine equivalent.Organic Letters 6, no. 10 (May 2004): 1653–56. https://doi.org/10.1021/ol049505a.
Baldwin, Steven W., and Alan Long. “2-tert-butyl-3-methyl-2,3-dihydroimidazol- 4-one-N-oxide: a new nitrone-based chiral glycine equivalent.Organic Letters, vol. 6, no. 10, May 2004, pp. 1653–56. Epmc, doi:10.1021/ol049505a.
Journal cover image

Published In

Organic letters

DOI

EISSN

1523-7052

ISSN

1523-7060

Publication Date

May 2004

Volume

6

Issue

10

Start / End Page

1653 / 1656

Related Subject Headings

  • Organic Chemistry
  • 34 Chemical sciences
  • 03 Chemical Sciences