Back to Search
Start Over
Stereoselective synthesis of 1,4-dideoxy-1,4-imino-d-allitol and formal synthesis of (2S,3R,4S)-3,4-dihydroxyproline
- Source :
-
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry . Jul2003, Vol. 44 Issue 30, p5641. 3p. - Publication Year :
- 2003
-
Abstract
- A stereoselective synthesis of 1,4-dideoxy-1,4-imino-d-allitol 1 and formal synthesis of (2S,3R,4S)-3,4-dihydroxyproline was achieved via the addition of vinylmagnesium bromide to the benzylimine derived from (R)-2,3-O-isopropylidene glyceraldehyde followed by N-allylation, ring-closing metathesis (RCM), and dihydroxylation. [Copyright &y& Elsevier]
- Subjects :
- *STEREOCHEMISTRY
*AROMATIC compounds
Subjects
Details
- Language :
- English
- ISSN :
- 00404039
- Volume :
- 44
- Issue :
- 30
- Database :
- Academic Search Index
- Journal :
- Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 10117548
- Full Text :
- https://doi.org/10.1016/S0040-4039(03)01366-2