Diastereoselective Addition of Organolithiums to New Chiral Hydrazones. Enantioselective Synthesis of (R)- Coniine
The reactions of organolithiums with the new chiral hydrazones derived from (S)-indoline-2-carboxylic acid afforded chiral hydrazines with Ugh diastereoselectivities (up to 99% de) and the present method was utilized for the preparation of high optically pure (R)-coniine (94% se). Copyright (C) 1996 Elsevier Science Ltd
- Publisher
- Pergamon-Elsevier Science Ltd
- Issue Date
- 1996-07
- Language
- English
- Article Type
- Article
- Keywords
ALDEHYDE-SAMP HYDRAZONES; ALPHA-AMINO ACIDS; ASYMMETRIC-SYNTHESIS; DIASTEREOFACIAL SELECTIVITY; GRIGNARD-REAGENTS; PIPERIDINES; ALKALOIDS; IMINES; ORGANOMETALLICS; (-)-CONIINE
- Citation
TETRAHEDRON LETTERS, v.37, no.31, pp.5543 - 5546
- ISSN
- 0040-4039
- Appears in Collection
- Files in This Item
- There are no files associated with this item.
This item is cited by other documents in WoS
| ⊙ Detail Information in WoSⓡ | Click to see |  |
| ⊙ Cited 69 items in WoS | Click to see citing articles in |  |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.