ChemInform Abstract: Diastereoselective and Enantioselective Intramolecular Amino-Zinc-Enolate Carbometalation Reactions. A New Polysubstiuted Pyrrolidine Synthesis.

ChemInform ◽  
2010 ◽  
Vol 29 (34) ◽  
pp. no-no
Author(s):  
E. LORTHIOIS ◽  
I. MAREK ◽  
J. F. NORMANT
Keyword(s):  
2001 ◽  
Vol 3 (26) ◽  
pp. 4169-4171 ◽  
Author(s):  
Sujen Lai ◽  
Charles K. Zercher ◽  
Jerry P. Jasinski ◽  
Seth N. Reid ◽  
Richard J. Staples

2013 ◽  
Vol 85 (6) ◽  
pp. 1149-1160 ◽  
Author(s):  
Minoru Isobe

Trimethylzincate is known to react through conjugate addition to α,β-unsaturated ketones, but adds much faster to α,β-unsaturated esters at low temperatures. Since the intermediate zinc enolate behaves differently from that of dimethylcuprate, it offers scope for application in a partial synthesis of gibberellin A3. A second example involving vinylsulfones having an oxygen atom on the γ-carbon strongly directs incoming nucleophiles in conjugate addition mode. Heteroatom-directed conjugate addition (HADCA) provides very reactive carbanion intermediates leading to cyclobutane ring formation, necessary for synthesis of solanoeclepin A. An alternative reaction for the four-membered carbocyclic ring closure was explored to make a bond formation between the propargylic cation of Nicholas type and allyltrimethylsilane nucleophile of Hosomi–Sakurai type. This method allowed a formation of tricyclo[5.2.1.01,6]decene framework.


2019 ◽  
Vol 60 (42) ◽  
pp. 151148
Author(s):  
Tetsuya Tsujihara ◽  
Moriho Tomeba ◽  
Shigeaki Ohkubo-Sato ◽  
Kyoko Iwabuchi ◽  
Rino Koie ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 30 (45) ◽  
pp. no-no
Author(s):  
Hyeon Kyu Lee ◽  
Jia Kim ◽  
Chwang Siek Pak
Keyword(s):  

ChemInform ◽  
2014 ◽  
Vol 45 (9) ◽  
pp. no-no
Author(s):  
Fei Ye ◽  
Zhan-Jiang Zheng ◽  
Wen-Hui Deng ◽  
Long-Sheng Zheng ◽  
Yuan Deng ◽  
...  

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