ChemInform Abstract: Stereoselective Reactions. Part 10. Total Synthesis of Optically Pure Antitumor Lignan, Burseran (I).

1986 ◽  
Vol 17 (16) ◽  
Author(s):  
K. TOMIOKA ◽  
T. ISHIGURO ◽  
K. KOGA
1985 ◽  
Vol 33 (10) ◽  
pp. 4333-4337 ◽  
Author(s):  
KIYOSHI TOMIOKA ◽  
TSUNEO ISHIGURO ◽  
KENJI KOGA

2015 ◽  
Vol 10 (1) ◽  
pp. 1934578X1501000
Author(s):  
Carmen Pérez Morales ◽  
M. Mar Herrador ◽  
José F. Quílez del Moral ◽  
Alejandro F. Barrero

Following the principles of collective total synthesis, a number of natural products sharing an optically pure, multifunctional, cyclopentanic core were synthesized from a common precursor: plinol A (1). This intermediate was efficiently obtained in only four steps from (-)-linalool (2) using as the key step a Ti(III)-mediated diastereoselective radical cyclization. The feasibility of this approach was confirmed with the expedient enantiospecific synthesis of cyclonerodiol (3), and the formal synthesis of chocol G (4) and piperitone (5).


1991 ◽  
Vol 28 (8) ◽  
pp. 1845-1847 ◽  
Author(s):  
Mieko Urano ◽  
Hitoshi Kagawa ◽  
Yoshihiro Harigaya ◽  
Shaoshun Li ◽  
Masayuki Onda

1994 ◽  
Vol 35 (22) ◽  
pp. 3733-3736 ◽  
Author(s):  
Masahide Tanaka ◽  
Hiroshi Mitsuhashi ◽  
Masao Maruno ◽  
Takeshi Wakamatsu

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