Catalytic Asymmetric Alkynylation of C1-Substituted C,N-Cyclic Azomethine Imines by CuI/Chiral Brønsted Acid Co-Catalyst

2011 ◽  
Vol 123 (38) ◽  
pp. 9114-9117 ◽  
Author(s):  
Takuya Hashimoto ◽  
Masato Omote ◽  
Keiji Maruoka
2011 ◽  
Vol 3 (8) ◽  
pp. 642-646 ◽  
Author(s):  
Takuya Hashimoto ◽  
Hidenori Kimura ◽  
Yu Kawamata ◽  
Keiji Maruoka

Synthesis ◽  
2018 ◽  
Vol 50 (10) ◽  
pp. 1935-1957 ◽  
Author(s):  
Daniel Sedgwick ◽  
Matthew Grayson ◽  
Santos Fustero ◽  
Pablo Barrio

The 50-year-old allylboration reaction has seen dramatic developments since the dawn of the new century after the first catalytic asymmetric versions came into play. In the past decade alone, several methodologies capable of achieving the desired homoallylic alcohols in over 90% ee have been developed. This review focuses on the chiral Brønsted acid catalyzed allylboration reaction, covering everything from the very first examples and precedents to modern day variations and applications.1 Introduction2 Early Developments3 Synthetic Applications4 Variants5 Computational Contribution6 Conclusions


2018 ◽  
Vol 91 (8) ◽  
pp. 1252-1257 ◽  
Author(s):  
Yukino Furukawa ◽  
Ryuhei Suzuki ◽  
Tsubasa Nakashima ◽  
Rafael Gramage-Doria ◽  
Kohsuke Ohmatsu ◽  
...  

Author(s):  
Yongbiao Guo ◽  
Zhenhua Gao ◽  
Junchen Li ◽  
Xiaojing Bi ◽  
Enxue Shi ◽  
...  

An efficient, practical and scalable protocol to prepare chiral 2,3-dihydroquinazolinones was developed under catalysis of spirocyclic SPINOL-phosphoric acid.


2014 ◽  
Vol 356 (16) ◽  
pp. 3451-3455 ◽  
Author(s):  
Shaolin Zhou ◽  
Steffen Fleischer ◽  
Haijun Jiao ◽  
Kathrin Junge ◽  
Matthias Beller

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