Recent Advances in Natural Product Synthesis by Using Intramolecular Diels—Alder Reactions

ChemInform ◽  
2006 ◽  
Vol 37 (17) ◽  
Author(s):  
Ken-ichi Takao ◽  
Ryosuke Munakata ◽  
Kin-ichi Tadano
2005 ◽  
Vol 105 (12) ◽  
pp. 4779-4807 ◽  
Author(s):  
Ken-ichi Takao ◽  
Ryosuke Munakata ◽  
Kin-ichi Tadano

ChemInform ◽  
2008 ◽  
Vol 39 (27) ◽  
Author(s):  
Paul G. Bulger ◽  
Sharan K. Bagal ◽  
Rodolfo Marquez

Molecules ◽  
2016 ◽  
Vol 21 (7) ◽  
pp. 951 ◽  
Author(s):  
Seung-Mann Paek ◽  
Myeonggyo Jeong ◽  
Jeyun Jo ◽  
Yu Heo ◽  
Young Han ◽  
...  

2021 ◽  
Vol 16 (10) ◽  
pp. 1934578X2110498
Author(s):  
Hisahiro Hagiwara

Recent advances in the total syntheses of cyclic natural products and related compounds from 2005 to 2021, which employ domino Michael reactions as key steps, have been reviewed, focusing mainly on the domino Michael reactions catalyzed by organocatalysts.


2018 ◽  
Vol 47 (21) ◽  
pp. 7926-7953 ◽  
Author(s):  
Baochao Yang ◽  
Shuanhu Gao

This review summarizes recent advances in Diels–Alder reactions involving o-QDMs, o-QMs and aza-o-QMs. The power and potential of this strategy in organic synthesis and natural product total synthesis is highlighted.


2018 ◽  
Vol 71 (9) ◽  
pp. 627
Author(s):  
Kieran D. Jones ◽  
Scott G. Stewart

The synthesis of steroids and gaining an ultimate understanding of their reactivity was one of Sir Derek Barton’s most notable research areas. This highlight will focus on the construction of the steroid ring system from 2016 to 2018, and will include pathways that eventually led to natural product synthesis. For example, efficient syntheses of ent-pregnanolone sulfate and oestradiol methyl ether will be explained along with the total synthesis of cannogenol-3-O-α-l-rhamnoside.


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