A method of producing an alcohol, comprises reducing an aldehyde or a ketone with a hydridosilatrane. The reducing is carried out with an activator.

The present invention provides amine salts of the prostacyclin analogue of Formula I

##STR00001##

and processes for generating these amine salts.

The present invention provides amine salts of the prostacyclin analogue of Formula I

##STR00001##

and processes for generating these amine salts.

The present invention provides amine salts of the prostacyclin analogue of Formula I

##STR00001##

and processes for generating these amine salts.

1,3-Dipole-functional compounds (e.g., azide functional compounds) can be reacted with certain alkynes in a cyclization reaction to form heterocyclic compounds. Useful alkynes (e.g., strained, cyclic alkynes) and methods of making such alkynes are also disclosed. The reaction of 1,3-dipole-functional compounds with alkynes can be used for a wide variety of applications including the immobilization of biomolecules on a substrate.

1,3-Dipole-functional compounds (e.g., azide functional compounds) can be reacted with certain alkynes in a cyclization reaction to form heterocyclic compounds. Useful alkynes (e.g., strained, cyclic alkynes) and methods of making such alkynes are also disclosed. The reaction of 1,3-dipole-functional compounds with alkynes can be used for a wide variety of applications including the immobilization of biomolecules on a substrate.

The present invention provides amine salts of the prostacyclin analogue of Formula I and processes for generating these amine salts. ##STR00001##

The present invention provides amine salts of the prostacyclin analogue of Formula I and processes for generating these amine salts. ##STR00001##

Provided are a tricyclodecane dimethanol composition, in which a ratio of isomers is controlled, and a preparation method thereof.

Provided are a tricyclodecane dimethanol composition, in which a ratio of isomers is controlled, and a preparation method thereof.