New Synthetic Route for the Enantioselective Total Synthesis of Salinosporamide A and Biologically Active Analogues

2005 ◽  
Vol 7 (13) ◽  
pp. 2699-2701 ◽  
Author(s):  
Leleti Rajender Reddy ◽  
Jean-François Fournier ◽  
B. V. Subba Reddy ◽  
E. J. Corey
ChemInform ◽  
2005 ◽  
Vol 36 (45) ◽  
Author(s):  
Leleti Rajender Reddy ◽  
Jean-Francois Fournier ◽  
B. V. Subba Reddy ◽  
E. J. Corey

Synthesis ◽  
2021 ◽  
Author(s):  
Keith P. Reber ◽  
Priyansh D. Gujarati

AbstractThe enantioselective total synthesis of the alkaloid aristoquinoline has been achieved in seven steps and 26% overall yield. A new preparation of the useful synthetic building block (–)-α-terpinyl amine was also developed in order to avoid stoichiometric mercury reagents or azide-containing intermediates. Key steps in the optimized synthetic route include an intramolecular nitrilium ion cyclization to form the characteristic azabicyclo[3.3.1]nonane ring system and a dia­stereoselective reduction of the resulting imine mixture to afford the natural product. An isomer of aristoquinoline containing an exocyclic alkene was also obtained and found to exhibit unusual chromatographic and spectroscopic properties.


2007 ◽  
Vol 9 (12) ◽  
pp. 2289-2292 ◽  
Author(s):  
Taotao Ling ◽  
Venkat R. Macherla ◽  
Rama Rao Manam ◽  
Katherine A. McArthur ◽  
Barbara C. M. Potts

ChemInform ◽  
2007 ◽  
Vol 38 (42) ◽  
Author(s):  
Taotao Ling ◽  
Venkat R. Macherla ◽  
Rama Rao Manam ◽  
Katherine A. McArthur ◽  
Barbara C. M. Potts

Author(s):  
Dongseok Jang ◽  
Minchul Choi ◽  
Jinglong Chen ◽  
Chulbom Lee

2021 ◽  
Author(s):  
Xin Shu ◽  
Chong-Chong Chen ◽  
Tao Yu ◽  
Jiayi Yang ◽  
Xiangdong Hu

2021 ◽  
Vol 67 ◽  
pp. 152895
Author(s):  
Shu Takahashi ◽  
Aoi Kimishima ◽  
Tomoyasu Hirose ◽  
Takeshi Yamada ◽  
Akihiro Sugawara ◽  
...  

Tetrahedron ◽  
2021 ◽  
Vol 87 ◽  
pp. 132110
Author(s):  
Gullapalli Kumaraswamy ◽  
Vankudoth Ramesh ◽  
Swargam Vijaykumar

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