## 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 ✦
Synthesis of Aminotetrazolyl Esters from Cyanogen Azide with Amino Esters
✍ Scribed by Joo, Young-Hyuk; Cho, Soo Gyeong; Goh, Eun Mee; Parrish, Damon A.; Shreeve, Jean'ne M.
- Book ID
- 118758313
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 490 KB
- Volume
- 2013
- Category
- Article
- ISSN
- 1434-193X
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