First Stereoselective Total Synthesis of Isoaspinonene through a Baylis-Hillman/Olefin Cross-Metathesis Protocol

2011 ◽  
Vol 2012 (3) ◽  
pp. 616-622 ◽  
Author(s):  
Palakodety Radha Krishna ◽  
Munagala Alivelu ◽  
Tadikamalla Prabhakar Rao
Synlett ◽  
2020 ◽  
Author(s):  
Debendra K. Mohapatra ◽  
Shivalal Banoth ◽  
Utkal Mani Choudhury ◽  
Kanakaraju Marumudi ◽  
Ajit C. Kunwar

AbstractA concise and convergent stereoselective synthesis of curvulone B is described. The synthesis utilized a tandem isomerization followed by C–O and C–C bond-forming reactions following Mukaiyama-type aldol conditions for the construction of the trans-2,6-disubstituted dihydropyran ring system as the key steps. Other important features of this synthesis are a cross-metathesis, epimerization, and Friedel–Crafts acylation.


Tetrahedron ◽  
2010 ◽  
Vol 66 (38) ◽  
pp. 7504-7509 ◽  
Author(s):  
Partha Ghosal ◽  
Vikas Kumar ◽  
Arun K. Shaw

Synthesis ◽  
2018 ◽  
Vol 51 (03) ◽  
pp. 780-786 ◽  
Author(s):  
Srinivas Kantevari ◽  
Santhosh Patpi ◽  
Guangyi Jin

The total synthesis of 5-hydroxygoniothalamin is achieved from commercially available l-xylose. The α,β-unsaturated-δ-lactone core is constructed in very good yield by utilizing one-carbon and two-carbon cis-Wittig olefinations and δ-lactonization using Yamaguchi conditions. Subsequent Grubbs cross-metathesis followed by desilylation results in 5-hydroxygoniothalamin.


2007 ◽  
Vol 79 (4) ◽  
pp. 677-684 ◽  
Author(s):  
Dominique Amans ◽  
Alexandre Le Flohic ◽  
Véronique Bellosta ◽  
Christophe Meyer ◽  
Janine Cossy

An analog of mycothiazole and pseudotrienic acid B were synthesized efficiently by using ring-closing metathesis or cross-metathesis as key reactions.


ChemInform ◽  
2014 ◽  
Vol 46 (3) ◽  
pp. no-no
Author(s):  
Arata Yajima ◽  
Akihiro Kawajiri ◽  
Ayaka Mori ◽  
Ryo Katsuta ◽  
Tomoo Nukada

2014 ◽  
Vol 97 (6) ◽  
pp. 868-880 ◽  
Author(s):  
Gandrath Dayaker ◽  
Palakodety Radha Krishna

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