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
APA
Chicago
ICMJE
MLA
NLM
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 SW, Long A. 2-tert-butyl-3-methyl-2,3-dihydroimidazol- 4-one-N-oxide: a new nitrone-based chiral glycine equivalent. Organic letters. 2004 May;6(10):1653–6.
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.
Baldwin SW, Long A. 2-tert-butyl-3-methyl-2,3-dihydroimidazol- 4-one-N-oxide: a new nitrone-based chiral glycine equivalent. Organic letters. 2004 May;6(10):1653–1656.
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