Abstract
Through mono-ester formation of 1,1′-bi-2-naphthol (BINOL) with pivaloyl chloride the selective mono-bromination was achieved cleanly on the other ring to afford 6-mono-bromo-1,1′-bi-2-naphthol in an efficient 86% yield.
Original language | English (US) |
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Pages (from-to) | 4055-4057 |
Number of pages | 3 |
Journal | Tetrahedron Letters |
Volume | 43 |
Issue number | 22 |
DOIs | |
State | Published - May 27 2002 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry
Keywords
- 6-mono-bromo-1,1′-bi-2-naphthol
- Bromination