Cu-Catalyzed [1,3]-Alkoxy Rearrangement/Diels–Alder Cascade Reactions via in Situ Generation of Functionalized ortho-Quinol Imines

2021 ◽  
Author(s):  
Itaru Nakamura ◽  
Kazuki Masukawa ◽  
Yasuhiro Ishida ◽  
Masahiro Terada
Synthesis ◽  
2021 ◽  
Author(s):  
Helena Armengol-Relats ◽  
Mauro Mato ◽  
Imma Escofet ◽  
Antonio Echavarren

The ability of highly energetic metal-carbene intermediates to engage in complex cascade or formal-cycloaddition processes is one of the most powerful tools for building intricate molecular architectures in a straightforward manner. Among this type of organometallic intermediates, non-acceptor metal carbenes are particularly challenging to access and, therefore, have experienced a slower development. In this regard, our group has exploited the use of electrophilic gold(I) complexes to selectively activate certain classes of substrates and generate this type of intermediates. Thus, very different type of molecules, such as enynes or 7-substituted cyclohepatrienes, lead to the formation of carbenes under gold(I) catalysis. Related rhodium(II) carbenes can also be generated from cyclohepatrienes. In this account, we aim to summarize our efforts towards the in-situ generation of these highly versatile organometallic species, and the study of their reactivity through formal cycloadditions or complex cascade reactions.


2012 ◽  
Vol 14 (23) ◽  
pp. 5940-5943 ◽  
Author(s):  
You-Cai Xiao ◽  
Qing-Qing Zhou ◽  
Lin Dong ◽  
Tian-Yu Liu ◽  
Ying-Chun Chen

ChemInform ◽  
2013 ◽  
Vol 44 (17) ◽  
pp. no-no
Author(s):  
You-Cai Xiao ◽  
Qing-Qing Zhou ◽  
Lin Dong ◽  
Tian-Yu Liu ◽  
Ying-Chun Chen

1991 ◽  
Vol 69 (1) ◽  
pp. 77-83 ◽  
Author(s):  
Gervais Bérubé ◽  
Alex G. Fallis

A general intramolecular Diels–Alder anionic oxy-Cope strategy for the synthesis of tricyclic skeletons and its application to the preparation of the gascardic acid precursor 21 is described. In situ generation of the appropriate cyclopentadiene 9 by isomerization (Et3N) afforded the [4+2] adduct directly or with EtAlCl2 as catalyst. The requisite potassium salt of the 1,5 diene 16 rearranged with concomitant epimerization at 67 °C to the fused ring ketone 18. Selective allylic oxidation and reduction provided 21. Key words: Diels–Alder, oxy-Cope, sesterterpene, synthesis, cycloaddition.


Sign in / Sign up

Export Citation Format

Share Document