scholarly journals Stereoselective Synthesis of Quaternary Carbons via the Dianionic Ireland–Claisen Rearrangement

2014 ◽  
Vol 16 (9) ◽  
pp. 2458-2461 ◽  
Author(s):  
Michael T. Crimmins ◽  
John D. Knight ◽  
Philip S. Williams ◽  
Yan Zhang
Keyword(s):  
Claisen Rearrangement ◽  
Stereoselective Synthesis ◽  
Quaternary Carbons

ChemInform Abstract: Stereoselective Synthesis of Quaternary Carbons via the Dianionic Ireland-Claisen Rearrangement.

ChemInform ◽  
2014 ◽  
Vol 45 (45) ◽  
pp. no-no
Author(s):  
Michael T. Crimmins ◽  
John D. Knight ◽  
Philip S. Williams ◽  
Yan Zhang
Keyword(s):  
Claisen Rearrangement ◽  
Stereoselective Synthesis ◽  
Quaternary Carbons

ChemInform Abstract: Highly Diastereoselective Claisen Rearrangement Leading to Vicinal Quaternary Carbons Construction of Oxindoles.

ChemInform ◽  
2012 ◽  
Vol 43 (10) ◽  
pp. no-no
Author(s):  
Yumiko Matsuta ◽  
Takayuki Kobari ◽  
Sachiko Kurashima ◽  
Yuhsuke Kumakura ◽  
Masashi Shinada ◽  
...  
Keyword(s):  
Claisen Rearrangement ◽  
Quaternary Carbons

A general and stereoselective synthesis of the capsaicinoids via the orthoester Claisen rearrangement

Tetrahedron ◽  
1996 ◽  
Vol 52 (25) ◽  
pp. 8451-8470 ◽  
Author(s):  
Harumi Kaga ◽  
Kouhei Goto ◽  
Tomiki Takahashi ◽  
Masao Hino ◽  
Takashi Tokuhashi ◽  
...  
Keyword(s):  
Claisen Rearrangement ◽  
Stereoselective Synthesis

Stereoselective synthesis of the viridiofungin analogue NA808 from a chiral tetrahydrofuran-carboxylic acid

2017 ◽  
Vol 15 (31) ◽  
pp. 6632-6639 ◽  
Author(s):  
Masatoshi Murakata ◽  
Takuma Ikeda
Keyword(s):  
Carboxylic Acid ◽  
Claisen Rearrangement ◽  
Stereoselective Synthesis

The viridiofungin analogue NA808 was synthesized by the stereoselective Ireland–Claisen rearrangement of dienylmethyl ester, regioselective bromolactonization of β-divinylpropanoic acid and retro-bromolactonization.

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