A Novel Stereoselective Access to Substituted l-2-Deoxypentono-1,4-lactones and l-2-Deoxypentoses
β Scribed by Dean V. Johnson; Roland Fischer; Herfried Griengl
- Book ID
- 108370998
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 131 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
1-(b-D -and a-L-Glycopyranosyl)-5-methyl-1H-1,2,4-triazoles 7, 13-15 were synthesized stereoselectively from the corresponding glycopyranosyl aminoguanidine nitrates 1-3 in boiling acetic anhydride or from N 1 -(acetylated b-Dor a-Lglycopyranosylamino)-N 1 ,N 2 ,N 3 -triacetylguanidines 8-10 using
A novel access to 1,4-benzodiazepin-2-ones starting from glycine and alanine derivatives is described. The key cyclization step was performed by the action of phenyliodine(III)bis(trifluoroacetate) (PIFA) on the corresponding methoxyamide derivatives leading to the C(9a) N(1) bond construction. This
## Abstract For Abstract see ChemInform Abstract in Full Text.