Conjugated ynones in catalytic enantioselective reactions

2021 ◽  
Vol 19 (10) ◽  
pp. 2110-2145
Author(s):  
Linqing Wang ◽  
Haiyong Zhu ◽  
Tianyu Peng ◽  
Dongxu Yang

This review summarizes the recent literature examples of catalytic asymmetric reactions of conjugated ynones and classified these reaction types, alongside their mechanistic insights whenever possible.

Author(s):  
Sara Meninno ◽  
Francesca Franco ◽  
Maurizio Benaglia ◽  
Alessandra Lattanzi

1998 ◽  
Vol 63 (4) ◽  
pp. 515-519 ◽  
Author(s):  
Štěpán Vyskočil ◽  
Martin Smrčina ◽  
Pavel Kočovský

Reductive alkylation of (R)-(+)-2,2'-diamino-1,1'-binaphthyl (1) with various ketones has been accomplished by means of NaBH4/H2SO4 in THF at room temperature. Bisalkylation predominated with the sterically less demanding acetone (1→3a; 82%), whereas the bulky 2-adamantanone afforded mainly the monoalkylated product 4c (71%). Both mono- and bisalkylated diamines (R)-3 and (R)-4 were reductively permethylated on reaction with CH2O, NaBH4, and H2SO4. The Pd(0)-catalyzed phenylation of (R)-(+)-1 with PhBr afforded the N,N'-diphenyl derivative (R)-7 (70%).


2020 ◽  
Vol 49 (18) ◽  
pp. 6755-6788 ◽  
Author(s):  
Abhijnan Ray Choudhury ◽  
Santanu Mukherjee

Deconjugated butenolides have emerged as a popular synthon for the enantioselective synthesis of γ-lactones. This review provides a comprehensive overview on the catalytic asymmetric reactions of deconjugated butenolides reported till date.


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