Double asymmetric iodoamination; Synthesis of C-2 symmetric and meso-amino alcohols
Alkenic diols 2 and 14 are iodocyclized providing dihydro-1,3-oxazine 3 and dihydrooxazole 15 in 90 and 93% de, respectively, which are precursors of various C-2 symmetric and meso-amino alcohols.
- Publisher
- ROYAL SOC CHEMISTRY
- Issue Date
- 1996-02
- Language
- English
- Article Type
- Article
- Keywords
HIV-1 PROTEASE INHIBITORS; STEREOCONTROLLED SYNTHESIS; CRYSTAL-STRUCTURE
- Citation
CHEMICAL COMMUNICATIONS, no.3, pp.355 - 356
- ISSN
- 1359-7345
- Appears in Collection
- CH-Journal Papers(저널논문)
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