Novel Group 6 Transition Metal Catalysts, MCl2(CO)3(AsPh3)2 (M=W, Mo), for the Metathesis Polymerization of Substituted Acetylenes

1998 ◽  
Vol 30 (7) ◽  
pp. 577-580 ◽  
Author(s):  
Hideo Nakako ◽  
Yoshihiko Misumi ◽  
Toshio Masuda ◽  
Lajos Bencze ◽  
Gabor Szalai
Keyword(s):  
Transition Metal ◽  
Metal Catalysts ◽  
Transition Metal Catalysts ◽  
Metathesis Polymerization ◽  
Group 6 ◽  
Substituted Acetylenes

scholarly journals One-pot synthesis of propynoates and propynenitriles

2017 ◽  
Vol 95 (2) ◽  
pp. 144-148 ◽  
Author(s):  
Fan Shu ◽  
Qingjuan Zheng ◽  
Wanrong Dong ◽  
Zhihong Peng ◽  
Delie An
Keyword(s):  
Low Temperature ◽  
Transition Metal ◽  
Functional Group ◽  
High Efficiency ◽  
Metal Catalysts ◽  
Transition Metal Catalysts ◽  
One Pot ◽  
Efficient Transformation ◽  
One Pot Synthesis ◽  
Substituted Acetylenes

An efficient transformation towards propynoates and propynenitriles is herein described. The practical methodology was conducted at low temperature (–78 or –60 °C) in a one-pot manner with the assistance of base rather than any transition metal catalysts. The base-induced protocol exhibits good functional group tolerance (up to 28 examples) and high efficiency (up to 92% yields) towards substituted acetylenes of great synthetic significance, which was also well demonstrated by the gram-scale reactions.

Sulfur-Mediated Reactions through Sulfonium Salts and Ylides

Synlett ◽  
2021 ◽  
Author(s):  
Pingfan Li
Keyword(s):  
Transition Metal ◽  
Rational Design ◽  
Acid Catalysis ◽  
Metal Catalysts ◽  
Transition Metal Catalysts ◽  
Bronsted Acid ◽  
Proof Of Concept ◽  
Sulfonium Salts ◽  
Brönsted Acid ◽  
Sulfonium Ylides

AbstractThis Account discusses several new reaction methods developed in our group that utilize sulfur-mediated reactions through sulfonium salts and ylides, highlighting the interplay of rational design and serendipity. Our initial goal was to convert aliphatic C–H bonds into C–C bonds site-selectively, and without the use of transition-metal catalysts. While a proof-of-concept has been achieved, this target is far from being ideally realized. The unexpected discovery of an anti-Markovnikov rearrangement and subsequent studies on difunctionalization of alkynes were much more straightforward, and eventually led to the new possibility of asymmetric N–H insertion of sulfonium ylides through Brønsted acid catalysis.1 Introduction2 Allylic/Propargylic C–H Functionalization3 Anti-Markovnikov Rearrangement4 Difunctionalization of Alkynes5 Asymmetric N–H Insertion of Sulfonium Ylides6 Conclusion

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