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P-stereogenic ligands in enantioselective catalysis /
P-stereogenic ligands were among the first to be used in asymmetric catalysis but synthetic difficulties and prejudices have hampered their development. However, continuous screening for new chiral ligands means that they can no longer be ignored and this rigorous reference source reflects their ren...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Cambridge :
Royal Society of Chemistry,
2010.
|
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
| LEADER | 00000cam a2200000 a 4500 | ||
|---|---|---|---|
| 001 | EBOOKCENTRAL_ocn710779758 | ||
| 003 | OCoLC | ||
| 005 | 20240329122006.0 | ||
| 006 | m o d | ||
| 007 | cr cnu---||||| | ||
| 008 | 110401s2010 enka o 000 0 eng | ||
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| 020 | |a 9781849732703 | ||
| 020 | |a 1849732701 | ||
| 029 | 1 | |a AU@ |b 000058156036 | |
| 029 | 1 | |a DEBBG |b BV044175223 | |
| 029 | 1 | |a DEBSZ |b 431414564 | |
| 035 | |a (OCoLC)710779758 | ||
| 050 | 4 | |a QD474 .G738 | |
| 082 | 0 | 4 | |a 547.12242 |
| 049 | |a UAMI | ||
| 100 | 1 | |a Grabulosa, Arnald. | |
| 245 | 1 | 0 | |a P-stereogenic ligands in enantioselective catalysis / |c Arnald Grabulosa. |
| 260 | |a Cambridge : |b Royal Society of Chemistry, |c 2010. | ||
| 300 | |a 1 online resource (501 pages) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 588 | 0 | |a Print version record. | |
| 505 | 0 | |a Introduction -- Resolution of racemic and diastereomeric mixtures -- P-stereogenic heterocycles -- P-stereogenic compounds derived from enantiopure heterocycles -- P-stereogenic phosphines prepared by enantioselective deprotonation -- Prepared by enantioselective catalysis -- Hydrogenation and related reactions -- Miscellaneous reactions. | |
| 520 | |a P-stereogenic ligands were among the first to be used in asymmetric catalysis but synthetic difficulties and prejudices have hampered their development. However, continuous screening for new chiral ligands means that they can no longer be ignored and this rigorous reference source reflects their renaissance. The book is filled with many examples from recent primary literature. The synthetic chemist will easily be able to follow the preparation methods which are accompanied by a description of the challenges and limitations. Those working in homogenous catalysis, and wanting to increase their r. | ||
| 590 | |a ProQuest Ebook Central |b Ebook Central Academic Complete | ||
| 650 | 0 | |a Ligands. | |
| 650 | 0 | |a Enantioselective catalysis. | |
| 650 | 6 | |a Ligands. | |
| 650 | 6 | |a Catalyse énantiosélective. | |
| 650 | 7 | |a Enantioselective catalysis |2 fast | |
| 650 | 7 | |a Ligands |2 fast | |
| 776 | 0 | 8 | |i Print version: |t P-stereogenic ligands in enantioselective catalysis. |d Cambridge : Royal Society of Chemistry, ©2010 |w (OCoLC)698593819 |
| 856 | 4 | 0 | |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=1186044 |z Texto completo |
| 994 | |a 92 |b IZTAP | ||