Abstract: Described herein are fungicidal compositions and methods of controlling and/or suppressing phytopathogenic fungi and fungus-like pathogens and maintaining crop health. Particularly described are fungicidal compositions and methods of controlling the phytopathogenic fungi and the Aphanomyces fungus-like pathogen and maintaining crop health in crops susceptible to infection.

Abstract: Described herein are fungicidal compositions and methods of controlling and/or suppressing phytopathogenic fungi and fungus-like pathogens and maintaining crop health. Particularly described are fungicidal compositions and methods of controlling the phytopathogenic fungi and the Aphanomyces fungus-like pathogen and maintaining crop health in crops susceptible to infection.

Abstract: Described herein are fungicidal compositions and methods of controlling and/or suppressing phytopathogenic fungi and fungus-like pathogens and maintaining crop health. Particularly described are fungicidal compositions and methods of controlling the phytopathogenic fungi and the Aphanomyces fungus-like pathogen and maintaining crop health in crops susceptible to infection.

Abstract: The present invention is a method of controlling or preventing unwanted vegetation in a crop planting site by applying a traditionally recognized post-emergent herbicide to a planting site in a pre-emergent application and subsequently applying the same or different traditionally recognized post-emergent herbicide to the planting site in a post-emergent application. Further, a reduction in the amount of a post-emergent herbicide necessary for controlling unwanted vegetation in a crop planting site can be achieved by providing a pre-emergent treatment including a traditionally recognized post-emergent herbicide to the planting site and subsequently providing a post-emergent treatment of a reduced amount of the same or different post-emergent herbicide.

Abstract: A process is claimed for preparing [1S(1(.alpha., 2.beta., 4.beta.)]-4-amino-2-hydroxymethyl -1-cyclopentanol from cis-4-((R)-benzoylamino)-2-cyclopentenecarboxylic acid, methyl ester in five steps. The invention also describes a number of novel intermediates useful in the synthesis of [1S(1.alpha., 2.beta.,4.beta.)]-4-amino-2-hydroxymethyl-1-cyclopentanol.