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Stereoselective synthesis of both enantiomers of trans-2-(diphenylmethylideneamino)cyclopropanecarboxylic acid using a chiral pool approach and their incorporation in dipeptides

Tamara Meiresonne (UGent) , Sven Mangelinckx (UGent) and Norbert De Kimpe (UGent)
(2012) TETRAHEDRON. 68(47). p.9566-9571
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Keywords
AMINOCYCLOPROPANE-CARBOXYLIC-ACIDS, ALPHA-AMINO-ACIDS, RING TRANSFORMATION, DERIVATIVES, PEPTIDES, CYCLOPROPANATION, ESTERS, CHEMISTRY, CATALYST

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Citation

Please use this url to cite or link to this publication:

MLA
Meiresonne, Tamara, Sven Mangelinckx, and Norbert De Kimpe. “Stereoselective Synthesis of Both Enantiomers of Trans-2-(diphenylmethylideneamino)cyclopropanecarboxylic Acid Using a Chiral Pool Approach and Their Incorporation in Dipeptides.” TETRAHEDRON 68.47 (2012): 9566–9571. Print.
APA
Meiresonne, T., Mangelinckx, S., & De Kimpe, N. (2012). Stereoselective synthesis of both enantiomers of trans-2-(diphenylmethylideneamino)cyclopropanecarboxylic acid using a chiral pool approach and their incorporation in dipeptides. TETRAHEDRON, 68(47), 9566–9571.
Chicago author-date
Meiresonne, Tamara, Sven Mangelinckx, and Norbert De Kimpe. 2012. “Stereoselective Synthesis of Both Enantiomers of Trans-2-(diphenylmethylideneamino)cyclopropanecarboxylic Acid Using a Chiral Pool Approach and Their Incorporation in Dipeptides.” Tetrahedron 68 (47): 9566–9571.
Chicago author-date (all authors)
Meiresonne, Tamara, Sven Mangelinckx, and Norbert De Kimpe. 2012. “Stereoselective Synthesis of Both Enantiomers of Trans-2-(diphenylmethylideneamino)cyclopropanecarboxylic Acid Using a Chiral Pool Approach and Their Incorporation in Dipeptides.” Tetrahedron 68 (47): 9566–9571.
Vancouver
1.
Meiresonne T, Mangelinckx S, De Kimpe N. Stereoselective synthesis of both enantiomers of trans-2-(diphenylmethylideneamino)cyclopropanecarboxylic acid using a chiral pool approach and their incorporation in dipeptides. TETRAHEDRON. 2012;68(47):9566–71.
IEEE
[1]
T. Meiresonne, S. Mangelinckx, and N. De Kimpe, “Stereoselective synthesis of both enantiomers of trans-2-(diphenylmethylideneamino)cyclopropanecarboxylic acid using a chiral pool approach and their incorporation in dipeptides,” TETRAHEDRON, vol. 68, no. 47, pp. 9566–9571, 2012.
@article{3263245,
  author       = {Meiresonne, Tamara and Mangelinckx, Sven and De Kimpe, Norbert},
  issn         = {0040-4020},
  journal      = {TETRAHEDRON},
  keywords     = {AMINOCYCLOPROPANE-CARBOXYLIC-ACIDS,ALPHA-AMINO-ACIDS,RING TRANSFORMATION,DERIVATIVES,PEPTIDES,CYCLOPROPANATION,ESTERS,CHEMISTRY,CATALYST},
  language     = {eng},
  number       = {47},
  pages        = {9566--9571},
  title        = {Stereoselective synthesis of both enantiomers of trans-2-(diphenylmethylideneamino)cyclopropanecarboxylic acid using a chiral pool approach and their incorporation in dipeptides},
  url          = {http://dx.doi.org/10.1016/j.tet.2012.09.078},
  volume       = {68},
  year         = {2012},
}

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