ChemInform Abstract: Enantio- and Diastereoselective Synthesis of Pipecolic Acid Derivatives Using the Aza-Diels-Alder Reaction of Imines with Dienes.

ChemInform ◽  
2010 ◽  
Vol 22 (33) ◽  
pp. no-no
Author(s):  
P. D. BAILEY ◽  
R. D. WILSON ◽  
G. R. BROWN
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Pipecolic Acid ◽  
Diastereoselective Synthesis ◽  
Diels Alder Reaction

scholarly journals Diastereoselective synthesis of novel spiro indanone fused pyrano[3,2-c]chromene derivatives following hetero-Diels–Alder reaction andin vitroanticancer studies

RSC Advances ◽  
2018 ◽  
Vol 8 (30) ◽  
pp. 16802-16814 ◽  
Author(s):  
Pravati Panda ◽  
Sabita Nayak ◽  
Susanta Ku. Sahoo ◽  
Seetaram Mohapatra ◽  
Deepika Nayak ◽  
...  
Keyword(s):  
Anticancer Activity ◽  
Alder Reaction ◽  
Diels Alder ◽  
Diastereoselective Synthesis ◽  
Diels Alder Reaction

Synthesis of novel spiro indanone fused pyrano[3,2-c]chromene derivatives following hetero-Diels–Alder reaction has been demonstrated and evaluated for theirin vitroanticancer activity.

Mechanochemical milling promoted solvent-free imino Diels–Alder reaction catalyzed by FeCl3: diastereoselective synthesis of cis-2,4-diphenyl-1,2,3,4-tetrahydroquinolines

RSC Advances ◽  
2014 ◽  
Vol 4 (67) ◽  
pp. 35635-35638 ◽  
Author(s):  
Ya-Jun Tan ◽  
Ze Zhang ◽  
Fang-Jian Wang ◽  
Hao-Hao Wu ◽  
Qing-Hai Li
Keyword(s):  
Ball Milling ◽  
Alder Reaction ◽  
Diels Alder ◽  
Solvent Free ◽  
Diastereoselective Synthesis ◽  
Diels Alder Reaction ◽  
Mechanochemical Milling

Cis-2,4-diphenyl-1,2,3,4-tetrahydroquinolines were diastereoselectively synthesized by FeCl3-promoted solvent-free Diels–Alder reaction of in situ generated imine with styrene under ball milling.

Diastereoselective Synthesis of Chiralcis-Annulated Polycyclic Heterocycles fromd-Glucose by Domino Knoevenagel-Hetero-Diels-Alder Reaction

Synthesis ◽  
2004 ◽  
Vol 2004 (08) ◽  
pp. 1150-1154 ◽  
Author(s):  
Gowravaram Sabitha ◽  
E. Venkata Reddy ◽  
Narjis Fatima ◽  
J. S. Yadav ◽  
K. V. Krishna ◽  
...  
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Diastereoselective Synthesis ◽  
Diels Alder Reaction

scholarly journals Oxidative Asymmetric Formal Aza-Diels–Alder Reactions of Tetrahydro-β-carboline with Enones in the Synthesis of Indoloquinolizidine-2-ones

Molecules ◽  
2018 ◽  
Vol 23 (9) ◽  
pp. 2228 ◽  
Author(s):  
Xiang Wu ◽  
Shi-Bao Zhao ◽  
Lang-Lang Zheng ◽  
You-Gui Li
Keyword(s):  
Oxidative Dehydrogenation ◽  
Alder Reaction ◽  
Diels Alder ◽  
Diastereoselective Synthesis ◽  
Butyl Hydroperoxide ◽  
Unsaturated Ketones ◽  
Tert Butyl ◽  
Diels Alder Reaction ◽  
Tert Butyl Hydroperoxide ◽  
Reaction Proceeds

Ru-catalyzed tandem amine oxidative dehydrogenation/formal aza-Diels–Alder reaction for enantio- and diastereoselective synthesis of indoloquinolizidine-2-ones from tetrahydro-β-carbolines and α,β-unsaturated ketones is described. The reaction proceeds via tandem ruthenium-catalyzed amine dehydrogenation using tert-butyl hydroperoxide (TBHP) as the oxidant and a chiral thiourea-catalyzed formal aza-[4 + 2] cycloaddition, providing a step-economical strategy for the synthesis of these valuable heterocyclic products.

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