Asymmetric Nucleophilic Addition Reactions of Aldehydes with Optically Active Dithioacetals and Their Application to Optically Active a-Hydroxy Ketone Synthesis

Heterocycles ◽  
2002 ◽  
Vol 57 (8) ◽  
pp. 1487 ◽  
Author(s):  
Ken-ichi Fujita ◽  
Hideo Taka ◽  
Akihiro Oishi ◽  
Yoichi Taguchi
Keyword(s):  
Nucleophilic Addition ◽  
Optically Active ◽  
Hydroxy Ketone ◽  
Addition Reactions

Stereoselective Nucleophilic Addition with a New Chiral Template and Its Application to the Synthesis of Optically Active α-Arylglycine Derivatives.

ChemInform ◽  
2004 ◽  
Vol 35 (37) ◽  
Author(s):  
Shigemitsu Tohma ◽  
Kentaro Rikimaru ◽  
Atsushi Endo ◽  
Keiko Shimamoto ◽  
Toshiyuki Kan ◽  
...  
Keyword(s):  
Nucleophilic Addition ◽  
Optically Active

scholarly journals Nucleophilic Addition Reactions of Nitriles to Nitrones under Mild Silylation Conditions

Synlett ◽  
2014 ◽  
Vol 25 (13) ◽  
pp. 1863-1868 ◽  
Author(s):  
Fumihiko Yoshimura ◽  
Keiji Tanino ◽  
Taiki Abe
Keyword(s):  
Nucleophilic Addition ◽  
Addition Reactions

Optically Active Nitroalkenes—Synthesis, Addition Reactions and Transformation into Amino Acids.

ChemInform ◽  
2003 ◽  
Vol 34 (19) ◽  
Author(s):  
Jan Huebner ◽  
Juergen Liebscher ◽  
Michael Paetzel
Keyword(s):  
Amino Acids ◽  
Optically Active ◽  
Addition Reactions

Amide-Directed Reactions of Small Carbocycles

2021 ◽  
Vol 25 ◽  
Author(s):  
Pavel M. Yamanushkin ◽  
Marina Rubina ◽  
Michael Rubin
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Nucleophilic Addition ◽  
Addition Reactions ◽  
Transition Metal Catalyzed ◽  
Metal Catalyzed

: The topic of this review is the amide-directed functionalization of strained carbocycles — specifically, unsaturated or saturated three- and four-membered rings. The following approaches are discussed: a) directed carbometallation and hydrometallation of cyclopropenes catalyzed by transition metals; b) directed metal-templated nucleophilic addition reactions; c) directed C-H functionalization, including transition metal-catalyzed C-H-activation reactions; and d) directed radical additions.

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