## Abstract 3‐Aryl‐3‐azido‐2‐hydroxypropanoic esters, prepared from the corresponding 3‐aryl‐oxirane‐2‐carboxylic esters by ring opening with sodium azide, were reduced with tin(II) chloride dihydrate in methanol to give 3‐amino‐3‐aryl‐2‐hydroxypropanoic esters in good yields. Under these condition
✦ LIBER ✦
An efficient synthesis of ?-diazo carboxylic esters from ?-amino carboxylic esters by base-catalysed of triazenes
✍ Scribed by McGarrity, John F.
- Book ID
- 120321154
- Publisher
- The Royal Society of Chemistry
- Year
- 1974
- Tongue
- English
- Weight
- 153 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0022-4936
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