Rearrangement of unactivated N-alkyl-O-benzoyl hydroxamic acid derivatives with phosphazene bases
โ Scribed by Andrew J Clark; Yassair S.S Al-Faiyz; Divya Patel; Michael J Broadhurst
- Book ID
- 104230144
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 72 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The phosphazene super bases BTPP 5, P-2-t Bu 6, and P-4-t Bu 7 mediate the rearrangement of unactivated N-alkyl-Obenzoyl hydroxamic acid derivatives 8, 11a-f, 13 and 16 to give 2-benzoyloxy amides 9, 12a-f, 14 and 17. The rate of reaction was found to be dependant upon the steric nature of the N-alkyl substituent.
๐ SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v
## Abstract The sodium salts of (__S__)โalanine, (__S__)โphenylalanine, (__S__)โvaline, and (__S__)โmethionine are condensed with pivalaldehyde to imines **5**. Cyclization by treatment with benzoyl chloride in cold CH~2~Cl~2~ gives mainly (4:1 to > 99:1) the (2__S__,4__S__)โ4โalkylโ3โbenzoylโ2โ(__