Synthesis of functionalized 5-substituted thiazolidine-2-thiones via adscititious xanthate-promoted radical cyclization of allyl(alkyl/aryl)dithiocarbamates

2016 ◽  
Vol 14 (3) ◽  
pp. 1002-1012 ◽  
Author(s):  
Simiao Gao ◽  
Yu Zhang ◽  
Jun Dong ◽  
Ning Chen ◽  
Jiaxi Xu

An adscititious radical precursor-promoted cyclization is designed and realized in efficient synthesis of functionalized 5-substituted thiazolidine-2-thiones from alkyl allyl(alkyl/aryl)dithiocarbamates.

1999 ◽  
Vol 23 (2) ◽  
pp. 164-165
Author(s):  
Goverdhan L. Kad ◽  
Anupam Khurana ◽  
Vasundhara Singh ◽  
Jasvinder Singh

Terpenoids 1 and 2 have been synthesized from readily available starting materials using Li2CuCI4-catalysed coupling of Grignard reagents with alkyl/aryl bromides and microwave-assisted oxidation of allylic methyl groups, using SeO2/ButOOH adsorbed over SiO2 as key steps.


2021 ◽  
Author(s):  
Sandeep Kumar ◽  
Sumit Kumar ◽  
Jyotirmoy Maity ◽  
Banty Kumar ◽  
Shilpika Bali ◽  
...  

Groebke-Blackburn-Bienayame (GBB) reaction has been used for the efficient synthesis of novel fluorescent 5-azaindolizino-2'-deoxyuridines starting from commercially available thymidine following two strategies. Thus, thymidine was converted to diacetylthymidine, which on...


2018 ◽  
Vol 57 (20) ◽  
pp. 5735-5739 ◽  
Author(s):  
Amol B. Gade ◽  
Pradip N. Bagle ◽  
Popat S. Shinde ◽  
Vipin Bhardwaj ◽  
Subhrashis Banerjee ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 33 (27) ◽  
pp. no-no
Author(s):  
S. Chandrasekhar ◽  
N. Ramakrishna Reddy ◽  
M. Venkat Reddy ◽  
B. Jagannadh ◽  
A. Nagaraju ◽  
...  

Synthesis ◽  
2020 ◽  
Vol 53 (02) ◽  
pp. 348-358
Author(s):  
Mikhail S. Novikov ◽  
Julia O. Strelnikova ◽  
Nikolai V. Rostovskii ◽  
Olesya V. Khoroshilova ◽  
Alexander F. Khlebnikov

AbstractA high-yielding method for the synthesis of 2H-1,3,5-oxadiazines by rhodium(II)- or copper(II)-catalyzed reaction of 1,2,4-oxadiazoles with α-diazo esters has been developed. The reaction proceeds via attack of the metallocarbenoid on the oxadiazole N2 atom followed by ring opening/1,6-electrocyclization and enables the introduction of alkyl, aryl, oxy, and amino substituents into the 6-position and electron-withdrawing groups into the 2-position of 1,3,5-oxadiazine. The N2-attack and the N4-attack of the carbenoid cause different oxadiazole ring openings, which are controlled by the substitution at C5. The presence of a substituent at this position is a prerequisite for the N2-attack to occur, leading to the formation of 1,3,5-oxadiazines.


2010 ◽  
Vol 8 (9) ◽  
pp. 2012 ◽  
Author(s):  
Mingcui Liu ◽  
Zeynab Hyder ◽  
Yawei Sun ◽  
Weijun Tang ◽  
Lijin Xu ◽  
...  

Synthesis ◽  
2008 ◽  
Vol 2008 (1) ◽  
pp. 94-100 ◽  
Author(s):  
Partha Chattopadhyay ◽  
Tirtha Majhi ◽  
Arpita Neogi ◽  
Soumen Ghosh ◽  
Alok Mukherjee ◽  
...  

2015 ◽  
Vol 17 (7) ◽  
pp. 3910-3915 ◽  
Author(s):  
Yangxin Wang ◽  
Chunshan Zhou ◽  
Ruihu Wang

An efficient catalytic protocol for hydroxylation of aryl halides in water is proposed to prepare phenols, ethers and benzofuran derivatives.


2018 ◽  
Vol 130 (20) ◽  
pp. 5837-5841 ◽  
Author(s):  
Amol B. Gade ◽  
Pradip N. Bagle ◽  
Popat S. Shinde ◽  
Vipin Bhardwaj ◽  
Subhrashis Banerjee ◽  
...  

2008 ◽  
Vol 19 (1) ◽  
pp. 184-193 ◽  
Author(s):  
Alex F. C. Flores ◽  
Darlene C. Flores ◽  
Graciela Oliveira ◽  
Lucas Pizzuti ◽  
Rubia M. S. da Silva ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document