Access to a guanacastepene and cortistatin-related skeleton via ethynyl lactone Ireland−Claisen rearrangement and transannular (4 + 3)-cycloaddition of an azatrimethylenemethane diyl
Heating a 2,5-furanocyclic (2-azidoethyl)allene initiates a cascade reaction comprising azide–allene cycloaddition, loss of nitrogen, and azatrimethylenemethane (ATMM) diyl–furan transannular (4+3)-cycloaddition. The major product of this reaction contains the pentacyclic core common to guanacastepe...
المؤلفون الرئيسيون: | Zhurakovskyi, O, Ellis, S, Thompson, A, Robertson, J |
---|---|
التنسيق: | Journal article |
منشور في: |
American Chemical Society
2017
|
مواد مشابهة
-
Synthesis of fused bicyclic medium-ring lactones via Claisen rearrangement
حسب: Burton, J, وآخرون
منشور في: (2000) -
Why do thioureas and squaramides slow down the Ireland–Claisen rearrangement?
حسب: Dominika Krištofíková, وآخرون
منشور في: (2019-12-01) -
Synthesis of medium-ring lactones via tandem methylenation/Claisen rearrangement of cyclic carbonates
حسب: Davidson, J, وآخرون
منشور في: (2000) -
Synthesis of medium-ring lactones via tandem methylenation/Claisen rearrangement of cyclic carbonates
حسب: Anderson, E, وآخرون
منشور في: (2002) -
Tandem RCM–Claisen Rearrangement–[2+2] Cycloaddition of O,O'-(But-2-en-1,4-diyl)-bridged Binaphthols
حسب: Michael Abraham, وآخرون
منشور في: (2012-12-01)