- Studies toward Diazonamide A: Development of a Hetero-Pinacol Macrocyclization Cascade for the Construction
- COMMUNICATIONS 834 WILEY-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002 1433-7851/02/4105-0834 $ 17.50+.50/0 Angew. Chem. Int. Ed. 2002, 41, No. 5
- Chemistry and Biology of Diazonamide A: First Total Synthesis and Confirmation of the True Structure
- Chem. Eur. J. 0000, 00, 0 0 DOI: 10.1002/chem.200400503 2004 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 1 K. C. Nicolaou et al.
- Natural Products Synthesis Chasing Molecules That Were Never There: Misassigned
- From Abyssomicin to Zaragozic Acid: Chemical Synthesis and Drug
- Regioselective aldol condensations of a cholestanone-derived dialdehyde: new twists on a classic reaction
- Natural Products DOI: 10.1002/anie.200703333
- Columbia Science Review24 Scott A. Snyder
- Concise Total Syntheses of Palominol, Dolabellatrienone, -Araneosene, and Isoedunol via an Enantioselective Diels-Alder Macrobicyclization
- Total Synthesis of Diazonamide A The Second Total Synthesis of Diazonamide A**
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- INTRODUCTION Gap junctions are intercellular protein channels formed by
- The essence of total synthesis K. C. Nicolaou* and Scott A. Snyder
- Tandem reactions, cascade sequences, and biomimetic strategies in total K. C. Nicolaou,ab Tamsyn Montagnona and Scott A. Snydera
- Acid Catalysis in Modern Organic
- 1. Introduction After numerous near-discoveries of the [42] cycloaddition
- Intramolecular Hetero DielsAlder Routes to g-Carboline Alkaloids
- Total Synthesis of Diazonamide A** K. C. Nicolaou,* Marco Bella, David Y.-K. Chen,
- Chemistry and Biology of Diazonamide A: Second Total Synthesis and Biological Investigations
- A New Method for the Stereoselective Synthesis of r-and -Glycosylamines Using the Burgess Reagent
- A New Method for the Synthesis of Nonsymmetrical Sulfamides Using Burgess-
- Studies toward Diazonamide A: Initial Synthetic Forays Directed toward the Originally Proposed Structure
