Iridium-Promoted Conversion of Chlorosilanes to Alkynyl Derivatives in a One-Pot Reaction Sequence

2014 ◽  
Vol 33 (12) ◽  
pp. 3051-3059 ◽  
Author(s):  
Ireneusz Kownacki ◽  
Bartosz Orwat ◽  
Bogdan Marciniec
Keyword(s):  
2013 ◽  
Vol 9 ◽  
pp. 974-982 ◽  
Author(s):  
Tamashree Ghosh ◽  
Abhishek Santra ◽  
Anup Kumar Misra

A series of glycosyl hemiacetal derivatives have been transformed into thioglycosides and glycosyl thiols in a one-pot two-step reaction sequence mediated by Appel reagent (carbon tetrabromide and triphenylphosphine). 1,2-trans-Thioglycosides and β-glycosyl thiol derivatives were stereoselectively formed by the reaction of the in situ generated glycosyl bromides with thiols and sodium carbonotrithioate. The reaction conditions are reasonably simple and yields were very good.


2015 ◽  
Vol 17 (4) ◽  
pp. 972-975 ◽  
Author(s):  
Feng Zhu ◽  
Peng-Wei Xu ◽  
Feng Zhou ◽  
Cui-Hong Wang ◽  
Jian Zhou
Keyword(s):  
One Pot ◽  

ChemInform ◽  
2008 ◽  
Vol 39 (38) ◽  
Author(s):  
J. S. Yadav ◽  
B. V. Subba Reddy ◽  
S. Aravind ◽  
G. G. K. S. Narayana Kumar ◽  
C. Madhavi ◽  
...  

2016 ◽  
Vol 358 (4) ◽  
pp. 526-531 ◽  
Author(s):  
Mélanie Decostanzi ◽  
Jérémy Godemert ◽  
Sylvain Oudeyer ◽  
Vincent Levacher ◽  
Jean-Marc Campagne ◽  
...  

2018 ◽  
Author(s):  
Martina Menger ◽  
Mathias Christmann

Here, we report a formal synthesis of the marine cytotoxic meroterpenoid actinoranone. Key steps include a racemization-free semipinacol rearrangement/Wittig reaction sequence and a chiral pool approach for the syntheses of the tetralone and the decalin fragments, respectively. The presented route provides access to the natural product in 14 steps in the longest linear sequence.


2020 ◽  
Vol 17 (10) ◽  
pp. 743-748
Author(s):  
Sultan Pathan ◽  
Anil Repale ◽  
Girdhar Pal

Celecoxib containing pyrazole derivatives were synthesized by path aldol condensation of substituted ketone with trifluoroethyl acetate subsequently by cyclization of the formed chalcones with 4-methanesulfonylphenylhydrazine. Here, a one-pot synthesis of celecoxib and substituted analogues have been reported which are nonsteroidal anti-inflammatory drugs for their cyclooxygenase (COX) inhibition, anti-inflammatory activity and ulcerogenic liability. In order to intermediate work-up, a continuous one-pot synthesis has been developed, performing the entire reaction sequence that results in a shorter time with good yield.


2010 ◽  
Vol 352 (5) ◽  
pp. 847-853 ◽  
Author(s):  
Chunyong Ding ◽  
Shanghui Tu ◽  
Qizheng Yao ◽  
Fulong Li ◽  
Yuanxiang Wang ◽  
...  

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