Axially chiral 1,1′-binaphthyls with non-identical groups in 2,2′-positions. Synthesis of the enantiomerically pure 2-hydroxy-2′-thiol and substituted 2-amino-2′-thiols
✍ Scribed by Martin Smrčina; Štěpán Vyskočil; Jana Polívková; Jana Poláková; Jan Sejbal; Vladimír Hanus; Miroslav Polášek; Hugh Verrier; Pavel Kočovský
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 708 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0957-4166
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✦ Synopsis
Enantiomerically pure hydroxy thiol (S)-(+)-6, amino thiol (S)-(+)-12, and N,N-dimethylamino thiol (S)-(-)-16 have been synthesized from BINOL (S)-(-)-1 and the amino alcohol (S)-(-)-7, respectively, via the Newman-Kwart rearrangement
📜 SIMILAR VOLUMES
A chiral complex of (R)-2-((pyridin-2-ylmethylene)amino)-2'-hydroxy-1,1'-binaphthyl (L) with hydrated nickel (II) acetate has been synthesized and spectroscopically characterized. The crystal structure of [NiL 2 (CH 3 OH)(CH 3 COO)]CH 3 COO•CH 3 OH has been determined by single-crystal X-ray diffrac