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Volumn 186, Issue 4, 2011, Pages 666-677

α-phosphino amino acids: Synthesis, structure, and reactivity

Author keywords

Asymmetric phosphines; Ethylene oligomerization; Hybrid ligands; Nickel catalysis; Phosphino amino acids

Indexed keywords


EID: 79955775804     PISSN: 10426507     EISSN: 15635325     Source Type: Journal    
DOI: 10.1080/10426507.2010.514485     Document Type: Conference Paper
Times cited : (15)

References (73)
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    • and references therein
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    • Gilbertson, S.R.1
  • 46
    • 0006904618 scopus 로고
    • DeutscherVerlag für Grundstoffindustrie: Leipzig, Germany
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    • Synthese, Struktur, Eigenschaften und Reaktivität unterschiedlich N-substituierter Phosphanylglycine,Ph.D. thesis; University of Greifswald, Germany
    • Lach, J. α-Phosphanyl-α-aminosäuren: Synthese, Struktur, Eigenschaften und Reaktivität unterschiedlich N-substituierter Phosphanylglycine, Ph.D. thesis; University of Greifswald, Germany, 2009.
    • (2009) α-Phosphanyl-α-aminosäuren
    • Lach, J.1
  • 69
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    • 221. The PM3 calculations were carried out with the program HYPERCHEM (Hypercube Inc.1993) using a root mean square gradient of 0.1 kcal/(Å•mol) and the Polak-Ribiere algorithm
    • Stewart, J. J. P. J. Comp. Chem. 1989, 10, 209, 221. The PM3 calculations were carried out with the program HYPERCHEM (Hypercube Inc. 1993) using a root mean square gradient of 0.1 kcal/(Å•mol) and the Polak-Ribiere algorithm.
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    • Stewart, J.J.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.