ChemInform Abstract: Natural Products Synthesis by Retro Diels-Alder Reaction. Part 12. Total Synthesis of Chromomoric Acid B (IX) and F Methyl Esters (XI).

ChemInform ◽  
2010 ◽  
Vol 26 (29) ◽  
pp. no-no
Author(s):  
X.-J. CHU ◽  
H. DONG ◽  
Z.-Y. LIU



ChemInform ◽  
2016 ◽  
Vol 47 (9) ◽  
pp. no-no
Author(s):  
Majid M. Heravi ◽  
Tahereh Ahmadi ◽  
Mahdieh Ghavidel ◽  
Bahareh Heidari ◽  
Hoda Hamidi


RSC Advances ◽  
2015 ◽  
Vol 5 (123) ◽  
pp. 101999-102075 ◽  
Author(s):  
Majid M. Heravi ◽  
Tahereh Ahmadi ◽  
Mahdieh Ghavidel ◽  
Bahareh Heidari ◽  
Hoda Hamidi

The synthetic utility and potential power of the Diels–Alder (D–A) reaction in organic chemistry is evident.



1984 ◽  
Vol 62 (2) ◽  
pp. 183-234 ◽  
Author(s):  
Alex G. Fallis

Recent advances and examples of the intramolecular Diels–Alder reaction are summarized and applications to the total synthesis of natural products, both completed and in progress, noted. A detailed discussion of trienes leading to bicyclo[4.3.0]nonene skeletons is followed by examples of bicyclo[4.4.0]decenes and adducts arising from ortho-quinodimethane precursors. Cycloadditions affording bicyclo[n.4.0] systems and bridged-ring adducts from cyclic dienes conclude this survey which is followed by a discussion of unreactive trienes and a brief analysis of synthetic strategy to complete the review.



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