Construction of tetralin skeletons based on rhodium-catalysed site-selective ring opening of benzocyclobutenols

2015 ◽  
Vol 51 (10) ◽  
pp. 1882-1885 ◽  
Author(s):  
Naoki Ishida ◽  
Norikazu Ishikawa ◽  
Shota Sawano ◽  
Yusuke Masuda ◽  
Masahiro Murakami

A rhodium complex induces site-selective alkene insertion into the C(sp2)–C(sp3) bond of benzocyclobutenols to furnish tetralins diastereoselectively.

2015 ◽  
Vol 17 (23) ◽  
pp. 5804-5807 ◽  
Author(s):  
Nuria Mazo ◽  
Iván García-González ◽  
Claudio D. Navo ◽  
Francisco Corzana ◽  
Gonzalo Jiménez-Osés ◽  
...  

ChemInform ◽  
2015 ◽  
Vol 46 (25) ◽  
pp. no-no
Author(s):  
Naoki Ishida ◽  
Norikazu Ishikawa ◽  
Shota Sawano ◽  
Yusuke Masuda ◽  
Masahiro Murakami

2021 ◽  
Vol 133 (19) ◽  
pp. 10893-10900
Author(s):  
Yanchao Wang ◽  
Maosheng Li ◽  
Shixue Wang ◽  
Youhua Tao ◽  
Xianhong Wang

Synthesis ◽  
2018 ◽  
Vol 51 (07) ◽  
pp. 1655-1661 ◽  
Author(s):  
Guang-Jian Mei ◽  
Feng Shi ◽  
Lei Yu ◽  
Zi-Qi Zhu ◽  
Meng Sun

An iridium-catalyzed branch-selective ring-opening reaction of vinylcyclopropanes with indoles has been established, which afforded C3-allylindoles in generally good to excellent yields (up to 95%). Considering that no wastes were generated in the whole process and branch-selective ring-opening reaction of vinylcyclopropanes was rarely reported, this strategy not only can be regarded as a highly atom-economic approach for C3-allylindoles, but also will greatly enrich the chemistry of vinylcyclopropanes.


Sign in / Sign up

Export Citation Format

Share Document