ChemInform Abstract: Asymmetric Synthesis. Part 25. Enantioselective Synthesis of Ethyl . beta.-Hydroxy-β-phenyl Propanoate via an Asymmetric Reformatsky Reaction.

ChemInform ◽  
2010 ◽  
Vol 27 (14) ◽  
pp. no-no
Author(s):  
A. MI ◽  
Z. WANG ◽  
Z. CHEN ◽  
Y. JIANG ◽  
A. S. C. CHAN ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Enantioselective Synthesis ◽  
Reformatsky Reaction

Asymmetric synthesis XXV: Enantioselective synthesis of ethyl β -hydroxy -β -phenyl propanoate via an asymmetric reformatsky reaction

1995 ◽  
Vol 6 (11) ◽  
pp. 2641-2642 ◽  
Author(s):  
Aiqiao Mi ◽  
Zhaoyang Wang ◽  
Zhenwan Chen ◽  
Yaozhong Jiang ◽  
Albert S.C. Chan ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Enantioselective Synthesis ◽  
Reformatsky Reaction

Enantioselective Functionalization of Prochiral Cyclobutanones and Cyclobutenones

Synlett ◽  
2021 ◽  
Author(s):  
Memg Wang ◽  
Changxu Zhong ◽  
Ping Lu
Keyword(s):  
Asymmetric Synthesis ◽  
Membered Ring ◽  
Enantioselective Synthesis ◽  
Ring Compounds ◽  
Recent Advances ◽  
Cyclobutane Derivatives

Enantioselective synthesis of cyclobutane derivatives is still a challenging topic in asymmetric synthesis. [2+2]-Cycloaddition and skeleton rearrangement are two primary strategies to this end. Recently, functionalization of cyclobutanones and cyclobutenones, which are readily available via [2+2]-cycloadditions as prochiral substrates, has emerged as a powerful tool to access versatile four-membered ring compounds. Herein, we summarize some recent advances in these areas from our and other groups.

scholarly journals Rhodium-catalyzed asymmetric synthesis of silicon-stereogenic silicon-bridged arylpyridinones

2016 ◽  
Vol 7 (2) ◽  
pp. 1205-1211 ◽  
Author(s):  
Ryo Shintani ◽  
Ryo Takano ◽  
Kyoko Nozaki
Keyword(s):  
Asymmetric Synthesis ◽  
Enantioselective Synthesis ◽  
Catalytic Cycle

A rhodium-catalyzed regio- and enantioselective synthesis of silicon-stereogenic silicon-bridged arylpyridinones was developed. A reasonable catalytic cycle was also experimentally established.

Enantioselective synthesis of α,α-difluoro-β-lactams using amino alcohol ligands

2014 ◽  
Vol 12 (33) ◽  
pp. 6484-6489 ◽  
Author(s):  
Atsushi Tarui ◽  
Takeshi Ikebata ◽  
Kazuyuki Sato ◽  
Masaaki Omote ◽  
Akira Ando
Keyword(s):  
Amino Alcohol ◽  
Enantioselective Synthesis ◽  
Reformatsky Reaction

A practical and highly enantioselective Reformatsky reaction of ethyl bromodifluoroacetate with imines using a cheap and commercially available amino alcohol ligand is described.

Asymmetric Synthesis of 6-Alkyl- and 6-Arylpiperidin-2-ones. Enantioselective Synthesis of (S)-(+)-Coniine

2007 ◽  
Vol 9 (13) ◽  
pp. 2473-2476 ◽  
Author(s):  
Stéphane Lebrun ◽  
Axel Couture ◽  
Eric Deniau ◽  
Pierre Grandclaudon
Keyword(s):  
Asymmetric Synthesis ◽  
Enantioselective Synthesis
Sign in / Sign up

Export Citation Format

Share Document