Synthesis of the First 2H-1,2-Azaphosphole Complexes with P,C and P,N Ylide Functional Groups
✍ Scribed by Rainer Streubel; Nils Hoffmann; H.-M. Schiebel; Frank Ruthe; Peter G. Jones
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 585 KB
- Volume
- 2002
- Category
- Article
- ISSN
- 1434-1948
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Synthetic procedures for N‐(2‐p–azidophenylethyl)‐norlevorphanol (9) labeled with ^14^C and ^3^H at the 1‐position of the 2‐phenylethyl moiety are presented. A process for synthesis of p‐nitrophenylacetic‐1‐^14^C acid from p‐chloro‐nitrobenzene and methyl cyano‐^14^C‐acetate is describe
Radical-initiated PϪH addition of (1S,2S)-C 5 H 8 (PH 2 ) 2 to cycloalkenes gave bis(secondary phosphanes), (1S,2S)-C 5 H 8 [P(H)C n H 2nϪ1 -cyclo] 2 (n = 5Ϫ8), as mixtures of R P ,R PЈ , S P ,S PЈ , and R P ,S PЈ diastereomers. The three diastereomers of the peralkylated chiral P 2 ligand