Enantioselective synthesis of rigid 2-aminotetralins. Utility of silicon as an oxygen and nitrogen surrogate in the tandem addition reaction.
Degnan, A P
Enantioselective synthesis of rigid 2-aminotetralins. Utility of silicon as an oxygen and nitrogen surrogate in the tandem addition reaction. [electronic resource] - The Journal of organic chemistry Jun 2000 - 3503-12 p. digital
Publication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
0022-3263
10.1021/jo0001131 doi
Antiparkinson Agents--chemical synthesis
Magnetic Resonance Spectroscopy
Nitrogen--chemistry
Oxygen--chemistry
Silicon--chemistry
Stereoisomerism
Tetrahydronaphthalenes--chemical synthesis
Enantioselective synthesis of rigid 2-aminotetralins. Utility of silicon as an oxygen and nitrogen surrogate in the tandem addition reaction. [electronic resource] - The Journal of organic chemistry Jun 2000 - 3503-12 p. digital
Publication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
0022-3263
10.1021/jo0001131 doi
Antiparkinson Agents--chemical synthesis
Magnetic Resonance Spectroscopy
Nitrogen--chemistry
Oxygen--chemistry
Silicon--chemistry
Stereoisomerism
Tetrahydronaphthalenes--chemical synthesis