Petri M. Pihko
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Petri M. Pihko has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
- Ari M. P. Koskinen
Department of Chemistry, Aalto University School of Chemical Technology, P. O. Box 16100 (Kemistintie 1), 00076 Aalto, Finland
1 shared publication Jan Tois
Laboratory of Organic Chemistry, Department of Chemical Technology, Helsinki University of Technology, FIN‐02015 HUT, Finland Fax:(+358)‐9‐451‐2538
1 shared publicationJatta E. Aho
Laboratory of Organic Chemistry, Helsinki University of Technology, P.O.B. 6100, FI-02015 HUT, Finland
1 shared publicationSami A. Selkälä
Laboratory of Organic Chemistry, Department of Chemical Technology, Helsinki University of Technology, FIN‐02015 HUT, Finland Fax:(+358)‐9‐451‐2538
1 shared publication
Latest Publications
- 11 September 2004
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 6 (21) , 3849-3852
Access to Both Anomers of Pectenotoxin Spiroketals by Kinetic Spiroketalization
A concise synthesis of both AB ring spiroisomers of the pectenotoxins is described. The nonanomeric AB spiroketal ring system of the pectenotoxins-1, -2, -3, and -6 is formed under very mild, kinetic spiroketalization conditions, along with the anomeric isomer. Only catalytic asymmetric transformations were used as the source of chirality in the synthesis route.
- 11 September 2004
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 6 (21) , 3849-3852
Access to Both Anomers of Pectenotoxin Spiroketals by Kinetic Spiroketalization
A concise synthesis of both AB ring spiroisomers of the pectenotoxins is described. The nonanomeric AB spiroketal ring system of the pectenotoxins-1, -2, -3, and -6 is formed under very mild, kinetic spiroketalization conditions, along with the anomeric isomer. Only catalytic asymmetric transformations were used as the source of chirality in the synthesis route.
- Top Cited Papers
- 6 April 2004
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 43 (16) , 2062-2064
Activation of Carbonyl Compounds by Double Hydrogen Bonding: An Emerging Tool in Asymmetric Catalysis
- 6 April 2004
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 43 (16) , 2062-2064
Top Cited PapersActivation of Carbonyl Compounds by Double Hydrogen Bonding: An Emerging Tool in Asymmetric Catalysis
- 6 April 2004
- Published by Wiley in Angewandte Chemie
- Vol. 116 (16) , 2110-2113
Carbonylaktivierung durch doppelte Wasserstoffbrückenbildung: ein neues Werkzeug für die asymmetrische Katalyse
- 6 April 2004
- Published by Wiley in Angewandte Chemie
- Vol. 116 (16) , 2110-2113
Carbonylaktivierung durch doppelte Wasserstoffbrückenbildung: ein neues Werkzeug für die asymmetrische Katalyse
- 1 October 2002
- Published by Wiley in Advanced Synthesis & Catalysis
- Vol. 344 (9) , 941-945
Asymmetric Organocatalytic Diels–Alder Reactions on Solid Support
- 1 October 2002
- Published by Wiley in Advanced Synthesis & Catalysis
- Vol. 344 (9) , 941-945
Asymmetric Organocatalytic Diels–Alder Reactions on Solid Support