Bovine serum albumin triggered waste-free aerobic oxidative coupling of thiols into disulphides on water: An extended synthesis of bioactive dithiobis(phenylene)bis(benzylideneimine) via sequential oxidative coupling–condensation reactions in one pot from aminothiophenol and benzaldehyde

2015 ◽  
Vol 116 ◽  
pp. 113-123 ◽  
Author(s):  
Saima ◽  
Aditya G. Lavekar ◽  
Rajesh Kumar ◽  
Arun K. Sinha
2013 ◽  
Vol 37 (11) ◽  
pp. 3731 ◽  
Author(s):  
Zhiming Chen ◽  
Zhenglian Xue ◽  
Lin Chen ◽  
Zhirong Geng ◽  
Renchun Yang ◽  
...  

ChemInform ◽  
2016 ◽  
Vol 47 (25) ◽  
Author(s):  
Kiran S. Dalal ◽  
Yogesh A. Tayade ◽  
Yogesh B. Wagh ◽  
Darshak R. Trivedi ◽  
Dipak S. Dalal ◽  
...  

Nanoscale ◽  
2021 ◽  
Author(s):  
Amit Nain ◽  
Hao-Hsin Huang ◽  
Daniel M. Chevrier ◽  
Yu-Ting Tseng ◽  
A. Sangili ◽  
...  

We report a one-pot facile synthesis of highly photoresponsive bovine serum albumin (BSA) templated bismuth-doped copper sulfide nanocomposites (BSA–BiZ/CuxS NCs, where BiZ represents in situ formed Bi2S3 and bismuth oxysulfides...


ChemCatChem ◽  
2016 ◽  
Vol 8 (19) ◽  
pp. 3050-3056 ◽  
Author(s):  
Yogesh Thopate ◽  
Richa Singh ◽  
Arun K. Sinha ◽  
Vikash Kumar ◽  
Mohammad Imran Siddiqi

RSC Advances ◽  
2019 ◽  
Vol 9 (48) ◽  
pp. 28228-28233
Author(s):  
Xiaoyu Zhang ◽  
Yandong Han ◽  
Zihao Xing ◽  
Zhenzhen Huang ◽  
Renguo Xie ◽  
...  

In this work, we demonstrated a facile, one-pot approach for preparation of gold nanoflowers by using tetrachloroauric acid as a gold precursor, ascorbic acid as a reductant, and bovine serum albumin (BSA) as a ligand.


2015 ◽  
Vol 7 (10) ◽  
pp. 4348-4354 ◽  
Author(s):  
Chun-Mei Li ◽  
Shou-Nian Ding

Dual-emitting bovine serum albumin–erbium(iii) complex-modulated gold–silver bimetallic nanoclusters (BSA–Er/Au/Ag-NCs) have been synthesized for the first time by a simple one-pot synthesis route.


2016 ◽  
Vol 14 (25) ◽  
pp. 6111-6118 ◽  
Author(s):  
Saima Saima ◽  
Danish Equbal ◽  
Aditya G. Lavekar ◽  
Arun K. Sinha

Bovine serum albumin–iodine acts as a cooperative catalyst for C(sp2)–H sulfenylation of indoles and hydroxyaryls (i.e. 2-naphthol/4-hydroxycoumarin) with diverse thiols (aryl/heteroaryl) using water under aerobic conditions.


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