(r)-(-)-5,5',6,6',7,7',8,8'-octahydro-3,3'-di-t-butyl-1,1'-bi-2-naphthol, dipotassium salt

(r)-(-)-5,5',6,6',7,7',8,8'-octahydro-3,3'-di-t-butyl-1,1'-bi-2-naphthol, dipotassium salt Structure
(r)-(-)-5,5',6,6',7,7',8,8'-octahydro-3,3'-di-t-butyl-1,1'-bi-2-naphthol, dipotassium salt structure
Common Name (r)-(-)-5,5',6,6',7,7',8,8'-octahydro-3,3'-di-t-butyl-1,1'-bi-2-naphthol, dipotassium salt
CAS Number 350683-75-9 Molecular Weight 482.78100
Density N/A Boiling Point N/A
Molecular Formula C28H36K2O2 Melting Point N/A
MSDS USA Flash Point N/A

A Readily Available and User-Friendly Chiral Catalyst for Efficient Enantioselective Olefin Metathesis This research was supported by the National Institutes of Health (GM-59426) and the National Science Foundation (CHE-9905806 to A. H. H. and CHE-9988766 to R. R. S.).

Angew. Chem. Int. Ed. Engl. 40 , 1452, (2001)

Efficient catalytic enantioselective synthesis of unsaturated amines: preparation of small- and medium-ring cyclic amines through mo-catalyzed asymmetric ring-closing metathesis in the absence of solvent.

J. Am. Chem. Soc. 124 , 6991, (2002)

The first catalytic asymmetric ring-closing metathesis method for the synthesis of N-containing heterocycles is reported; this is accomplished through Mo-catalyzed kinetic resolution or desymmetrization of unsaturated amines. Importantly, this catalytic asymm...

S.L. Aeilts et al.

Angew. Chem. Int. Ed. Engl. 113 , 1500, (2001)