Giovanni Casiraghi
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Giovanni Casiraghi has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
Gloria Rassu
Istituto per l'Applicazione delle Tecniche Chimiche Avanzate ai Problemi Agrobiologici del CNR, Via Vienna 2, I-07100 Sassari, Italy
2 shared publications- Franca Zanardi
Department of Food and Drug University of Parma Parma Italy
1 shared publication - Lucia Battistini
Department of Food and Drug University of Parma Parma Italy
1 shared publication - Luigi Pinna
Dipartimento di Chimica e Farmacia Università di Sassari Via Vienna 2 07100 Sassari Italy
1 shared publication
Latest Publications
- 1 February 1999
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 10 (4) , 765-773
Diastereoselective synthesis of a novel lactam peptidomimetic exploiting vinylogous Mannich addition of 2-silyloxyfuran reagents
- 1 February 1999
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 10 (4) , 765-773
Diastereoselective synthesis of a novel lactam peptidomimetic exploiting vinylogous Mannich addition of 2-silyloxyfuran reagents
- 1 June 1995
- Published by Georg Thieme Verlag KG in Synthesis
- Vol. 1995 (06) , 607-626
Furan-, Pyrrole-, and Thiophene-Based Siloxydienes for Syntheses of Densely Functionalized Homochiral Compounds
This review describes the methods of preparation and use of 2-(trimethylsiloxy)furan, N-(tert-butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole, and certain substituted analogues and congeners, including novel 2-(tert-butyldimethylsiloxy)thiophene, to synthesize complex carbohydrates, azasugars, polyhydroxylated alkaloids, C-glycosylated α-amino acids, amino acids bearing quaternary chiral carbon atoms, and thiosugars. Especially emphasized is the preparation of enantiomerically pure compounds of biological interest. Some mechanistic insights are presented.
- 1 June 1995
- Published by Georg Thieme Verlag KG in Synthesis
- Vol. 1995 (06) , 607-626
Furan-, Pyrrole-, and Thiophene-Based Siloxydienes for Syntheses of Densely Functionalized Homochiral Compounds
This review describes the methods of preparation and use of 2-(trimethylsiloxy)furan, N-(tert-butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole, and certain substituted analogues and congeners, including novel 2-(tert-butyldimethylsiloxy)thiophene, to synthesize complex carbohydrates, azasugars, polyhydroxylated alkaloids, C-glycosylated α-amino acids, amino acids bearing quaternary chiral carbon atoms, and thiosugars. Especially emphasized is the preparation of enantiomerically pure compounds of biological interest. Some mechanistic insights are presented.