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4361 - 4370 von 4591

	4361	Ring Closing Enyne Metathesis: Control over Mode Selectivity and Stereoselectivity. Enthalten in ChemInform Bd. 36, 2005, Nr. 8: no-no. 1 S.
	4362	Ring Closing Enyne Metathesis: Control over Mode Selectivity and Stereoselectivity. Enthalten in ChemInform Bd. 36, 2005, Nr. 8: no-no. 1 S.
	4363	Ring‐Closing Metathesis Approach to a 16‐Membered Macrocycle of Kendomycin. Enthalten in ChemInform Bd. 38, 2007, Nr. 45: no-no. 1 S.
	4364	Ring‐Closing Metathesis Approach to Dictyostatin. Enthalten in ChemInform Bd. 36, 2005, Nr. 25: no-no. 1 S.
	4365	Ring‐Closing Metathesis as a Basis for the Construction of Aromatic Compounds Enthalten in ChemInform Bd. 37, 2006, Nr. 30: no-no. 1 S.
	4366	Ring‐Closing Metathesis as a Construct for the Synthesis of Polycyclic Alkaloids Enthalten in ChemInform Bd. 37, 2005, Nr. 1: no-no. 1 S.
	4367	Ring-closing metathesis as key step in the synthesis of Luffarin I, 16-epi-Luffarin I and Luffarin A Enthalten in Molecular diversity Bd. 20, 20.10.2015, Nr. 2, date:5.2016: 369-377
	4368	Ring‐Closing Metathesis Dimerizations of Enynes and Deprotections of Propargyl Ethers Mediated by Carbene Ruthenium Complexes. Enthalten in ChemInform Bd. 36, 2005, Nr. 18: no-no. 1 S.
	4369	Ring‐Closing Metathesis for the Synthesis of 2H‐ and 4H‐Chromenes. Enthalten in ChemInform Bd. 37, 2006, Nr. 5: no-no. 1 S.
	4370	Ring‐Closing Metathesis in Biphasic BMI×PF 6 Ionic Liquid/Toluene Medium: A Powerful Recyclable and Environmentally Friendly Process. Enthalten in ChemInform Bd. 36, 2005, Nr. 13: no-no. 1 S.

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