Synthesis of highly hindered 1,2-diaryl diketones and of cis- and trans-1,2-diacetoxy-1,2-bis(aryl)ethenes
Highly hindered 1,2-diaryl diketones can be synthesized in good yields by the reaction of 1-aryllithium with CO in THF solution at atmospheric pressure; preparation of cis- and trans-1,2-diacetoxy-1,2-bis(Mes)ethene can be also afforded by a similar procedure and further quenching with Ac2O.
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| Formato: | Capítulo de libro |
| Lenguaje: | Inglés |
| Publicado: |
Royal Society of Chemistry
1999
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| Acceso en línea: | Registro en Scopus DOI Handle Registro en la Biblioteca Digital |
| Aporte de: | Registro referencial: Solicitar el recurso aquí |
| LEADER | 03941caa a22006377a 4500 | ||
|---|---|---|---|
| 001 | PAPER-19635 | ||
| 003 | AR-BaUEN | ||
| 005 | 20230518205059.0 | ||
| 008 | 190411s1999 xx ||||fo|||| 00| 0 eng|d | ||
| 024 | 7 | |2 scopus |a 2-s2.0-0032828048 | |
| 024 | 7 | |2 cas |a carbon monoxide, 630-08-0 | |
| 040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
| 030 | |a JRPSD | ||
| 100 | 1 | |a Nudelman, N. | |
| 245 | 1 | 0 | |a Synthesis of highly hindered 1,2-diaryl diketones and of cis- and trans-1,2-diacetoxy-1,2-bis(aryl)ethenes |
| 260 | |b Royal Society of Chemistry |c 1999 | ||
| 270 | 1 | 0 | |m Nudelman, N.; Departamento de Quimica Organica, Facultad Ciencias Exactas Naturales, Universidad de Buenos Aires, Pab. II, P. 3, C. Universitaria, 1428 Buenos Aires, Argentina |
| 506 | |2 openaire |e Política editorial | ||
| 504 | |a Trost, B.M., Fleming, I., (1993) Comprehensive Organic Synthesis, , Pergamon Press, New York, ch. 9 | ||
| 504 | |a Wirth, T., (1996) Angew. Chem., Int. Ed. Engl., 35, p. 61 | ||
| 504 | |a Tomaselli, G.A., Failla, S., Ballisteri, F.P., (1988) J. Org. Chem., 53, p. 830 | ||
| 504 | |a Karaman, R., Fry, J., (1989) Tetrahedron Lett., 30, p. 2757 | ||
| 504 | |a Katritzky, A.R., Wang, Z., Lang, H., Feng, D., (1997) J. Org. Chem., 62, p. 4125 | ||
| 504 | |a Kohler, E.P., Baltzly, R., (1932) J. Am. Chem. Soc., 54, p. 4015 | ||
| 504 | |a Nudelman, N.S., Doctorovich, F., (1994) Tetrahedron, 50, p. 4651 | ||
| 504 | |a Seyferth, D., Weinstein, R., (1982) J. Am. Chem. Soc., 104, p. 5534. , or thioesters | ||
| 504 | |a Seyferth, D., Hul, R., (1984) Organometallics, 3, p. 327 | ||
| 504 | |a Schleyer, P.V.R., Winchester, W.R., Bauer, W., (1987) Organometallics, 6, p. 2371 | ||
| 504 | |a note; Nudelman, N.S., Vitale, A.A., (1983) J. Organomet. Chem., 241, p. 143 | ||
| 504 | |a Toda, F., (1995) Acc. Chem. Res., 28, p. 480 | ||
| 504 | |a Nudelman, N.S., Vitale, A.A., (1981) Org. Prep. Proced., 13, p. 144 | ||
| 504 | |a Nudelman, N.S., Lewcowicz, E.S., Perez, D.G., (1990) Synthesis, p. 917 | ||
| 504 | |a Fuson, R.C., Scott, S.L., Horning, E.C., McKeever, C., (1940) J. Am. Chem. Soc., 62, p. 2091 | ||
| 504 | |a Shacklett, C.D., Smieth, H.A., (1953) J. Am. Chem. Soc., 75, p. 2654 | ||
| 504 | |a Cook, J.W., (1930) J. Chem. Soc., p. 1087 | ||
| 504 | |a Fuson, R.C., McKeever, C.H., Corse, J., (1940) J. Am. Chem. Soc., 72, p. 600 | ||
| 520 | 3 | |a Highly hindered 1,2-diaryl diketones can be synthesized in good yields by the reaction of 1-aryllithium with CO in THF solution at atmospheric pressure; preparation of cis- and trans-1,2-diacetoxy-1,2-bis(Mes)ethene can be also afforded by a similar procedure and further quenching with Ac2O. |l eng | |
| 593 | |a Depto. de Quim. Orgánica, Fac. de Ciencias Exactes y Naturales, Universidad de Buenos Aires, Pab. II, P. 3, 1428 Buenos Aires, Argentina | ||
| 690 | 1 | 0 | |a 1,2 DICARBONYL DERIVATIVE |
| 690 | 1 | 0 | |a CARBON MONOXIDE |
| 690 | 1 | 0 | |a ETHYLENE DERIVATIVE |
| 690 | 1 | 0 | |a LITHIUM DERIVATIVE |
| 690 | 1 | 0 | |a ARTICLE |
| 690 | 1 | 0 | |a CIS TRANS ISOMERISM |
| 690 | 1 | 0 | |a CROSS LINKING |
| 690 | 1 | 0 | |a STEREOSPECIFICITY |
| 690 | 1 | 0 | |a SYNTHESIS |
| 700 | 1 | |a Schulz, H. | |
| 773 | 0 | |d Royal Society of Chemistry, 1999 |h pp. 422-423 |k n. 7 |p J. Chem. Res. Part S |x 03082342 |w (AR-BaUEN)CENRE-2560 |t Journal of Chemical Research - Part S | |
| 856 | 4 | 1 | |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032828048&doi=10.1039%2fa809045i&partnerID=40&md5=6f98391a12e20a5a106e26c910f07efe |y Registro en Scopus |
| 856 | 4 | 0 | |u https://doi.org/10.1039/a809045i |y DOI |
| 856 | 4 | 0 | |u https://hdl.handle.net/20.500.12110/paper_03082342_v_n7_p422_Nudelman |y Handle |
| 856 | 4 | 0 | |u https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03082342_v_n7_p422_Nudelman |y Registro en la Biblioteca Digital |
| 961 | |a paper_03082342_v_n7_p422_Nudelman |b paper |c PE | ||
| 962 | |a info:eu-repo/semantics/article |a info:ar-repo/semantics/artículo |b info:eu-repo/semantics/publishedVersion | ||
| 999 | |c 80588 | ||