Efficient method for preparation of N-methoxy-N-methyl amides by reaction of lactones or esters with Me2AlClMeONHMe·HCl
- 1 April 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (15) , 2685-2688
- https://doi.org/10.1016/s0040-4039(97)00429-2
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Synthetic studies on reveromycin A: Stereoselective synthesis of the spiroketal systemTetrahedron Letters, 1996
- 1,3-Stereocontrol with Bromoallenes. Synthesis of N-Boc-ADDA, the Unique Amino Acid Present in Several Inhibitors of Serine/Threonine PhosphatasesThe Journal of Organic Chemistry, 1996
- Synthetic studies on tautomycin. Stereoselective construction of the C1–C26 regionTetrahedron Letters, 1994
- Enantioselective synthesis of (−)-serricornin, a sex pheromone of a female cigarette beetle (Lasioderma serricorne F.)Tetrahedron: Asymmetry, 1993
- Total synthesis of the ionophore antibiotic X-206. Studies relevant to the stereoselective synthesis of the C(17)–C(26) synthon.Tetrahedron Letters, 1986
- An Alternative Procedure for the Aluminum-Mediated Conversion of Esters to AmidesSynthetic Communications, 1982
- N-methoxy-n-methylamides as effective acylating agentsTetrahedron Letters, 1981
- A mild, general method for conversion of esters to amidesTetrahedron Letters, 1977