Organic Reactions in Aqueous Media. Cyclopentadienylindium(I) as the First Example of Organoindium(I) Reagent for Carbon−Carbon Bond Formation and the Demonstration of One-Pot Tandem Addition/Intramolecular Diels−Alder Reaction in Aqueous Media

2000 ◽  
Vol 122 (2) ◽  
pp. 402-403 ◽  
Author(s):  
Yang ◽  
Tak Hang Chan
2006 ◽  
Vol 59 (5) ◽  
pp. 340 ◽  
Author(s):  
Anthony R. Lingham ◽  
Helmut M. Hügel ◽  
Trevor J. Rook

Salvinorin A 1, a psychoactive neoclerodane diterpenoid from the Mexican sage S. divinorum, has gained interest as a selective κ-opioid receptor agonist. Non-racemic 3-furylamines 9a and 9b have been prepared from (+)-pseudoephedrine and (–)-ephedrine for application in the stereoselective synthesis of the ketone ring of 1. Diels–Alder reaction of 9b with methyl acrylate in aqueous media, followed by selective ether bridge cleavage, has allowed access to the cyclohexenone 17 with preservation of stereochemistry at C2. A model route to the lactone ring has also been achieved through a one-pot deconjugation/esterification procedure of 2-bromocrotonyl chloride 20 to the furyl alcohol 19 followed by Reformatski-mediated ring closure.


2014 ◽  
Vol 126 (5) ◽  
pp. 1369-1371 ◽  
Author(s):  
SAMBASIVARAO KOTHA ◽  
SHAIBAL BANERJEE ◽  
MOBIN SHAIKH

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