A concise, stereoselective synthesis of meso-2,6-diaminopimelic acid (DAP)
摘要:
The preparation of meso-2,6-diaminopimelic acid 1 is described. The key step in the synthesis is Suzuki coupling of the novel organoboron homoalanine equivalent 3 with methyl (2Z)-3-bromo-2-[(tert-butoxycarbonyl)amino]-2-propenoate 5. (C) 2001 Elsevier Science Ltd. All rights reserved.
The hetero Diels-Alder adducts 6a-d derived from azodibenzoyl and cyclic dienes were oxidized by ruthenium tetroxide and transformed into meso-diaminodicarboxylic acids 12a-d via the new cyclic hydrazoacetic acids 9a-d.
Bricas,E. et al., Bulletin de la Societe Chimique de France, 1965, p. 1813 - 1818
作者:Bricas,E. et al.
DOI:——
日期:——
van Heijenoort,J. et al., Bulletin de la Societe Chimique de France, 1969, p. 2743 - 2747
作者:van Heijenoort,J. et al.
DOI:——
日期:——
A concise, stereoselective synthesis of meso-2,6-diaminopimelic acid (DAP)
作者:Philip N Collier、Ian Patel、Richard J.K Taylor
DOI:10.1016/s0040-4039(01)01150-9
日期:2001.8
The preparation of meso-2,6-diaminopimelic acid 1 is described. The key step in the synthesis is Suzuki coupling of the novel organoboron homoalanine equivalent 3 with methyl (2Z)-3-bromo-2-[(tert-butoxycarbonyl)amino]-2-propenoate 5. (C) 2001 Elsevier Science Ltd. All rights reserved.