Concave Reagents, 15 [1] . New Concave 1,10‐Phenanthrolines: Catalysts for the Alcohol Addition to Ketenes and Ligands in Transition Metal Complexes-Reference-Cited by-同舟云学术

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Concave Reagents, 15 [1] . New Concave 1,10‐Phenanthrolines: Catalysts for the Alcohol Addition to Ketenes and Ligands in Transition Metal Complexes

Published:1994-11 Issue:11 Volume:127 Page:2297-2306
ISSN:0009-2940
Container-title:Chemische Berichte
language:en
Short-container-title:Chem. Ber.

Author:

Lüning Ulrich¹,Müller Michael²,Gelbert Markus¹,Peters Karl³,Schnering Hans Georg Von²,Keller Manfred²

Affiliation:

1. Institut für Organische Chemie der Universität Kiel, Olshausenstraße 40, D‐24098 Kiel, Germany

2. Chemisches Laboratorium der Universität Freiburg, Albertstraße 21, D‐79104 Freiburg, Germany

3. Max‐Planck‐Institut für Festkörperforschung, Heisenbergstraße 1, D‐70506 Stuttgart, Germany

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.1491271131

Reference44 articles.

1. Concave reagents - 14. Concave pyridines with a 2,6-diarylpyridine core.

2. [2a]U.Lüning Liebigs Ann. Chem.1987 949–955.

3. — [b]U.Lüning R.Baumstark K.Peters H. G. v.Schnering Liebigs Ann. Chem.1990 129–143.

4. — [c]U.Lüning R.Baumstark M.Müller Liebigs Ann. Chem.1991 987–998.

5. U.Lüning M.Müller Liebigs Ann. Chem.1989 367–374.

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2. ChemInform Abstract: Concave Reagents. Part 15. New Concave 1,10-Phenanthrolines: Catalysts for the Alcohol Addition to Ketenes and Ligands in Transition Metal Complexes;ChemInform;2010-08-18

3. Towards Allosteric Receptors â Synthesis of Resorcinarene-Functionalized 2,2â²-Bipyridines and Their Metal Complexes;European Journal of Organic Chemistry;2009-10

4. Benzoaza-15-crown-5 ethers: synthesis, structure, and complex formation with metal and ethylammonium ions;Russian Chemical Bulletin;2009-05

5. Concave 1,10-Phenanthrolines as Ligands for Cyclopropanations - Towards a Deeper Understanding of the Stereoselectivity;European Journal of Organic Chemistry;2009-05

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