EFFICIENT SYNTHESIS OF EXO-1-AZABICYCLO[2.2.1]HEPTAN-3-OL
暂无分享,去创建一个
S. Barrett | H. Tecle | J. Jaén | B. Caprathe | A. Thomas
[1] D. Hughes,et al. PROGRESS IN THE MITSUNOBU REACTION. A REVIEW , 1996 .
[2] M. Brann,et al. (±)-1-Azabicyclo[2.2.1]heptan-3-one, O-(3-methyl-5-aryl-2-penten-4-ynyl) oximes: Potent muscarinic agonists , 1995 .
[3] M. Brann,et al. In vitro and in vivo evaluation of the subtype-selective muscarinic agonist PD 151832. , 1995, Life sciences.
[4] G. Riley,et al. Design and synthesis of novel muscarinic agonists containing the 1,2,4-triazine ring as an ester bioisostere , 1994 .
[5] R. Bernotas,et al. The use of triphenylphosphine/diethyl azodicarboxylate (DEAD) for the cyclization of 1,4- and 1,5-amino alcohols , 1991 .
[6] C. Swain,et al. Novel 5-HT3 antagonists. Indole oxadiazoles. , 1991, Journal of medicinal chemistry.
[7] D. Spry,et al. Azabicyclic alcohols. VI. Azabicyclo [2.2.1]heptan-3-ol epimers , 1969 .
[8] K. Hasse,et al. Zur Darstellung von Δ1-Pyrrolin-carbonsäure-(2) und eine neue Prolinsynthese , 1960 .
[9] V. Mićović,et al. The Reduction of Acid Amides with Lithium Aluminum Hydride , 1953 .