azaspiracid and nonane

azaspiracid has been researched along with nonane* in 1 studies

Other Studies

1 other study(ies) available for azaspiracid and nonane

Article	Year
Synthesis of a 2,9-dioxabicyclo[3.3.1]nonane via double intramolecular hetero-Michael addition: entry to the F-G ring system of the azaspiracids. Organic letters, 2001, Apr-05, Volume: 3, Issue:7 [structure: see text]. An effective approach to form a 1,3-disubstituted 2,9-dioxabicyclo[3.3.1]nonane system representing the core of the F and G rings (C28-C34) of the azaspiracid natural products has been developed. The double intramolecular hetero-Michael addition (DIHMA) of a diol upon an ynone generated the bicyclic ketal in a highly diastereoselective fashion. Topics: Alkanes; Bridged Bicyclo Compounds; Isomerism; Marine Toxins; Molecular Structure; Oxidation-Reduction; Spiro Compounds; Water	2001

Article

Year

Synthesis of a 2,9-dioxabicyclo[3.3.1]nonane via double intramolecular hetero-Michael addition: entry to the F-G ring system of the azaspiracids.

Organic letters, 2001, Apr-05, Volume: 3, Issue:7

[structure: see text]. An effective approach to form a 1,3-disubstituted 2,9-dioxabicyclo[3.3.1]nonane system representing the core of the F and G rings (C28-C34) of the azaspiracid natural products has been developed. The double intramolecular hetero-Michael addition (DIHMA) of a diol upon an ynone generated the bicyclic ketal in a highly diastereoselective fashion.

Topics: Alkanes; Bridged Bicyclo Compounds; Isomerism; Marine Toxins; Molecular Structure; Oxidation-Reduction; Spiro Compounds; Water

2001