Phosphitylation via the Mitsunobu reaction
โ Scribed by I.Darren Grice; Peta J. Harvey; Ian D. Jenkins; Michael J. Gallagher; Millagahamada G. Ranasinghe
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- French
- Weight
- 160 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Alkylation of Pyrazolones via the Mitsunobu Reaction. -Mitsunobu coupling of pyrazolinone (I) or 4-acylated analogues with simple alcohols results in a preferred or exclusive O-alkylation depending on the solvent used. This mild and effective method allows the preparation of products which are not
AIbslBlmL-2-Amidophenol attached to a solid support can be converted to the corresponding benzoxazole by treatment with tdphenylphosphine and diathyl azodicarboxylate in THF at room temperature in high yield and purity. ยฉ 1997 l~lsevk~ ~ยข~mcยข Lt(L The synthesis and screening of small molecule combin