Regio- and stereoselective rearrangements of formyl [2.2.1]bicyclic carbinols in methanol

Yang, Te‐Fang; Tseng, Chih-Hao; Shen, Chien-Hung; Chen, Li-Hsun; Kao, L. Glenn

doi:10.1016/j.tet.2009.09.057

Cited by 11 publications

(2 citation statements)

References 19 publications

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“…This reaction is however normally found to occur for basic compounds. In addition to some reasonably described methodologies, 44,45,46 Nunsubstituted, i.e NH-1,2,3-triazoles can also be prepared by hydrogenolysis of Nbenzylsubstituted 1,2,3-triazoles in the presence of palladium on carbon. A report by…”

Section: Debenzylation Of N-benzyl 4-and 5-substituted 123-triazlesmentioning

confidence: 99%

1,3-Dipolar cycloaddition of benzyl azide to two highly functionalized alkynes

et al. 2011

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Section: Debenzylation Of N-benzyl 4-and 5-substituted 123-triazlesmentioning

confidence: 99%

1,3-Dipolar cycloaddition of benzyl azide to two highly functionalized alkynes

et al. 2011

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“…The latter would then undergo a stereoselective nucleophilic addition with a second equivalent of the organometallic reagent to give the products 381a , b after hydrolysis. Similar acid-catalyzed nonalkylative rearrangements of 379a , b have been described more recently …”

Section: Bicylo[321] Ring System From Polycyclic Precursorsmentioning

confidence: 99%