Unravelling transition metal-catalyzed terpenic alcohol esterification: a straightforward process for the synthesis of fragrances

2016 ◽  
Vol 6 (9) ◽  
pp. 3197-3207 ◽  
Author(s):  
M. J. da Silva ◽  
D. A. M. Ayala

Iron nitrate, a simple and commercially available Lewis acid, catalyzes terpenic alcohol esterification with acetic acid, achieving high conversion and ester selectivity.

2001 ◽  
pp. 151-155
Author(s):  
Kenichiro NISHIWAKI ◽  
Hidehiro MATSUDA ◽  
Katsumi ISHIGE ◽  
Kyoji AOKI

1992 ◽  
Vol 21 (7) ◽  
pp. 1141-1142 ◽  
Author(s):  
Takahiro Nishiguchi ◽  
Kazuyuki Nakata ◽  
Ken Takaki ◽  
Yuzo Fujiwara

2018 ◽  
Vol 90 (4) ◽  
pp. 723-731 ◽  
Author(s):  
Susanne Bähr ◽  
Martin Oestreich

AbstractSeveral approaches toward electrophilic C–H silylation of electron-rich arenes are discussed, comprising transition-metal-catalyzed processes as well as Lewis-acid- and Brønsted-acid-induced protocols. These methods differ in the catalytic generation of the silicon electrophile but share proton removal in form of dihydrogen. With slight modifications, these methods are often also applicable to the related electrophilic C–H borylation.


Synthesis ◽  
2020 ◽  
Vol 52 (06) ◽  
pp. 819-833 ◽  
Author(s):  
Jen-Chieh Hsieh ◽  
Haw-Lih Su

The diverse methodologies to synthesize N-heterocycles through transition-metal-catalyzed cascade addition/cyclization of a nitrile are discussed in this review. Aspects relating to three types of transition-metal-catalyzed addition of a nitrile with subsequent cyclization include (1) a transition-metal acting as a Lewis acid to accelerate the nucleophilic addition of a nitrile, (2) the late-transition-metal-catalyzed 1,2-insertion of a nitrile, and (3) an in situ generated radical by transition-metal catalysis to implement a radical addition/cyclization tandem reaction. Applications for the synthesis of natural alkaloids, their derivatives, and some bioactive compounds are also summarized herein.1 Introduction2 Nucleophilic Addition of a Nitrile Accelerated by a Lewis Acid2.1 Late-Transition-Metal Catalysis2.2 Early-Transition-Metal Catalysis2.3 Lanthanide-Metal Catalysis2.4 Cyclization from N-Arylnitriliums3 Transition-Metal-Catalyzed Insertion of a Nitrile4 Transition-Metal-Catalyzed Radical Addition of a Nitrile5 Conclusions


2019 ◽  
Vol 25 (60) ◽  
pp. 13785-13798
Author(s):  
Yinwu Li ◽  
Jiahao Liu ◽  
Xiao Huang ◽  
Ling‐Bo Qu ◽  
Cunyuan Zhao ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 24 (11) ◽  
pp. no-no
Author(s):  
T. NISHIGUCHI ◽  
K. NAKATA ◽  
K. TAKAKI ◽  
Y. FUJIWARA

2020 ◽  
Vol 7 (8) ◽  
pp. 1022-1060 ◽  
Author(s):  
Wenbo Ma ◽  
Nikolaos Kaplaneris ◽  
Xinyue Fang ◽  
Linghui Gu ◽  
Ruhuai Mei ◽  
...  

This review summarizes recent advances in C–S and C–Se formations via transition metal-catalyzed C–H functionalization utilizing directing groups to control the site-selectivity.


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