182416-69-9Relevant academic research and scientific papers
2,3,5-TRISUBSTITUTED TETRAHYDROFURANS BY Rh-MEDIATED CYCLISATION OF AN α-DIAZO ESTER
Taber, Douglass F.,Song, Ying
, p. 2587 - 2590 (1995)
Dirhodium(II) carboxylate catalyzed cyclization of a γ-alkoxy-α-diazo ester 1 was found to proceed with substatial diastereoselectivity, producing the 2,3,5-trisubstituted tetrahydrofurans 2a and 2b in a ratio of 4:1.
Diastereoselective Rh-mediated construction of 2,3,5-trisubstituted tetrahydrofurans
Taber, Douglass F.,Song, Ying
, p. 6706 - 6712 (2007/10/03)
Dirhodium(II) carboxylate catalyzed cyclization of a series of γ-alkoxy-α-diazo esters 1 has been shown to proceed with substantial diastereoselectivity, producing the 2,3,5-trisubstituted tetrahydrofurans 2 and 3. The diastereoselectivity of the cyclizat
