scholarly journals A New Protocol for the in situ Generation of Aromatic, Heteroaromatic, and Unsaturated Diazo Compounds and Its Application in Catalytic and Asymmetric Epoxidation of Carbonyl Compounds. Extensive Studies to Map Out Scope and Limitations, and Rationalization of Diastereo- and Enantioselectivities.

ChemInform ◽  
2004 ◽  
Vol 35 (2) ◽  
Author(s):  
Varinder K. Aggarwal ◽  
et al. et al.
2016 ◽  
Vol 40 (12) ◽  
pp. 10300-10304 ◽  
Author(s):  
Raktani Bikshapathi ◽  
Parvathaneni Sai Prathima ◽  
Vaidya Jayathirtha Rao

An efficient, eco-friendly protocol for selective oxidation of primary and secondary Baylis–Hillman alcohols to the corresponding carbonyl compounds in high yields has been developed with 2-iodosobenzoic acid (IBA).


2016 ◽  
Vol 14 (45) ◽  
pp. 10723-10732 ◽  
Author(s):  
Jijun Chen ◽  
Ying Shao ◽  
Liang Ma ◽  
Meihua Ma ◽  
Xiaobing Wan

A novel in situ generation of nitrilium from nitrile ylide and the subsequent Mumm rearrangement of carboxylic acid, nitrile, and diazo compounds gave various unsymmetrical diacylglycine esters.


ACS Catalysis ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 2940-2948 ◽  
Author(s):  
Dan Wu ◽  
Willinton Y. Hernández ◽  
Songwei Zhang ◽  
Evgeny I. Vovk ◽  
Xiaohong Zhou ◽  
...  

Synthesis ◽  
2021 ◽  
Author(s):  
Chhanda Mukhopadhyay ◽  
Sayan Pramanik ◽  
Suman Ray ◽  
Suvendu Maity ◽  
Prasanta Ghosh

AbstractAn efficient diastereoselective trans cyclopropanation of 3-alkylidene oxindoles with in situ generated α-diazo carbonyl compounds or α,β-unsaturated diazo compounds under metal-free conditions has been developed to synthesize 3-spirocyclopropyl-2-oxindole derivatives. The procedure is based on the 1,3-dipolar character of the corresponding diazo compounds under base-catalyzed conditions. The method has a wide substrate scope and uses easily available starting materials.


RSC Advances ◽  
2013 ◽  
Vol 3 (36) ◽  
pp. 15608 ◽  
Author(s):  
Naoki Morimoto ◽  
Shun-ichi Yamamoto ◽  
Yasuo Takeuchi ◽  
Yuta Nishina

2018 ◽  
Vol 54 (94) ◽  
pp. 13256-13259 ◽  
Author(s):  
Emmanuelle M. D. Allouche ◽  
Afnan Al-Saleh ◽  
André B. Charette

The modular synthesis of a variety of trans 1,2-disubstituted cyclopropanes in a one-pot iron-catalyzed cyclopropanation is described. N-nosylhydrazones are used as diazo precursors, allowing the in situ generation of electron-rich diazo compounds and their direct participation in the reaction.


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