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Results: 1-6 |
Results: 6

Authors: Guarna, A Menchi, G Berti, G Cini, N Bottoncetti, A Raspanti, S Politi, A Pupi, A
Citation: A. Guarna et al., Synthesis and preliminary biological characterization of a new potential I-125-radioligand for dopamine and serotonin receptors, BIO MED CH, 9(12), 2001, pp. 3197-3206

Authors: Machetti, F Ferrali, A Menchi, G Occhiato, EG Guarna, A
Citation: F. Machetti et al., Oligomers of enantiopure bicyclic gamma/delta-amino acids (BTAa). 1. Synthesis and conformational analysis of 3-aza-6,8-dioxabicyclo[3.2.1]octane-7-carboxylic acid oligomers (PolyBTG), ORG LETT, 2(25), 2000, pp. 3987-3990

Authors: Menchi, G Scrivanti, A Matteoli, U
Citation: G. Menchi et al., Improvements in the synthesis of terminal alkynes via coupling of arylbromides with 2-methylbut-3-yn-2-ol, J MOL CAT A, 152(1-2), 2000, pp. 77-82

Authors: Guarna, A Guidi, A Machetti, F Menchi, G Occhiato, EG Scarpi, D Sisi, S Trabocch, A
Citation: A. Guarna et al., Synthesis and reactivity of bicycles derived from tartaric acid and alpha-amino acids: A novel class of conformationally constrained dipeptide isosteres based upon enantiopure 3-aza-6,8-dioxabicyclo[3.2.1]octane-7-carboxylicacid. (vol 64, pg 7358, 1995), J ORG CHEM, 65(15), 2000, pp. 4782-4782

Authors: Guarna, A Guidi, A Machetti, F Menchi, G Occhiato, EG Scarpi, D Sisi, S Trabocchi, A
Citation: A. Guarna et al., Synthesis and reactivity of bicycles derived from tartaric acid and alpha-amino acids: A novel class of conformationally constrained dipeptide isosteres based upon enantiopure 3-aza-6,8-dioxabicyclo[3.2.1]octane-7-carboxylicacid, J ORG CHEM, 64(20), 1999, pp. 7347-7364

Authors: Staccioli, G Sturaro, A Parvoli, G Menchi, G Matteoli, U
Citation: G. Staccioli et al., The lipophilic extractives of an interglacial fossil Picea abies from Zeifen (Germany), HOLZFORSCH, 53(4), 1999, pp. 391-396
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