scholarly journals P-chiral 1-phosphanorbornenes: from asymmetric phospha-Diels–Alder reactions towards ligand design and functionalisation

2016 ◽  
Vol 45 (5) ◽  
pp. 1904-1917 ◽  
Author(s):  
Tobias Möller ◽  
Peter Wonneberger ◽  
Menyhárt B. Sárosi ◽  
Peter Coburger ◽  
Evamarie Hey-Hawkins
Keyword(s):  
Ligand Design ◽  
Diels Alder ◽  
Chiral Auxiliary ◽  
Building Set ◽  
Ligand Synthesis

A building set for chiral phosphorus. The principle of stereotopic face differentiation is successfully applied to a PC bond. A divergent ligand synthesis is feasible after reduction of the chiral auxiliary.

Endo-benzonorbornen-2-ol as an efficient non-natural chiral auxiliary in the asymmetric aza-Diels–Alder reactions between cyclopentadiene and (1-phenylethyl)iminoacetates

RSC Advances ◽  
2014 ◽  
Vol 4 (101) ◽  
pp. 57768-57772 ◽  
Author(s):  
Carlos A. D. Sousa ◽  
Miguel A. Maestro ◽  
Xerardo Garcia-Mera ◽  
José E. Rodríguez-Borges
Keyword(s):  
Diels Alder ◽  
Chiral Auxiliary

A chiral auxiliary derived from levoglucosenone in asymmetric Diels–Alder transformations

2005 ◽  
Vol 46 (41) ◽  
pp. 6987-6990 ◽  
Author(s):  
Ariel M. Sarotti ◽  
Rolando A. Spanevello ◽  
Alejandra G. Suárez
Keyword(s):  
Diels Alder ◽  
Chiral Auxiliary

ChemInform Abstract: Asymmetric Hetero Diels-Alder Reaction of Nitroso Compounds Utilizing Tartaric Acid Ester as a Chiral Auxiliary.

ChemInform ◽  
2009 ◽  
Vol 40 (18) ◽  
Author(s):  
Hiroki Sakai ◽  
Xia Ding ◽  
Tetsusuke Yoshida ◽  
Shuhei Fujinami ◽  
Yutaka Ukaji ◽  
...  
Keyword(s):  
Tartaric Acid ◽  
Acid Ester ◽  
Alder Reaction ◽  
Diels Alder ◽  
Chiral Auxiliary ◽  
Nitroso Compounds ◽  
Diels Alder Reaction
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