Molecular diversity of the acid promoted domino reaction of 3-hydroxy-3-(indol-3-yl)indolin-2-ones and cyclic mercapto-substituted β-enamino esters

2021 ◽  
Author(s):  
Liu-Na Pan ◽  
Qing Wang ◽  
Jing Sun ◽  
Quan-Shun Sun ◽  
Chao-Guo Yan

The acetic acid promoted reaction of 3-hydroxy-3-(indol-3-yl)indolin-2-ones and mercapto-substituted β-enamino esters showed very interesting molecular diversity.

2019 ◽  
Vol 43 (22) ◽  
pp. 8644-8650 ◽  
Author(s):  
Mohit Saroha ◽  
Jitender M. Khurana

Acetic acid mediated regioselective synthesis of novel 2,4,5-trisubstituted thiazole derivatives has been reported by a domino reaction of thiosemicarbazide and aldehydes/ketones/isatin, to generate thiosemicarbazones (in situ) followed by addition of arylglyoxal and active methylene/activated C–H acids/pyrazole/indole in ethanol at 80 °C.


2015 ◽  
Vol 42 (5) ◽  
pp. 4759-4772 ◽  
Author(s):  
Ahmad Reza Moosavi-Zare ◽  
Mohammad Ali Zolfigol ◽  
Ehsan Noroozizadeh ◽  
Omid Khaledian ◽  
Behzad Shirmardi Shaghasemi

Synlett ◽  
2021 ◽  
Author(s):  
Chunmei Li ◽  
Furen Zhang ◽  
Zhenlu Shen

A three-component domino reaction for the synthesis of naphtho[2,3-b][1,6]naphthyridine derivatives has been established. Such strategy exhibited excellent substrate scope including various enaminones and aldehydes afforded a series of multi-functionalized naphtho[2,3-b][1,6]naphthyridine derivatives with 70-86% yields. The advantages of bond-forming efficiency, accessibility of starting materials and water as sole by-products provide invaluable access to biological 1,6-naphthyridines.


RSC Advances ◽  
2017 ◽  
Vol 7 (7) ◽  
pp. 3928-3933 ◽  
Author(s):  
Ruchi Bharti ◽  
Pooja Kumari ◽  
Tasneem Parvin ◽  
Lokman H. Choudhury

The three-component reaction of 2-hydroxy-1,4-naphthaquinone, aldehydes, and 6-aminouracil derivatives in acetic acid/water (1 : 1; v/v) under microwave and conventional heating conditions are reported.


Author(s):  
N.C. Lyon ◽  
W. C. Mueller

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.


2001 ◽  
Vol 120 (5) ◽  
pp. A153-A153
Author(s):  
S MIYAMOTO ◽  
K KATO ◽  
Y ISHII ◽  
S ASAI ◽  
T NAGAISHI ◽  
...  

2004 ◽  
Vol 171 (4S) ◽  
pp. 94-94
Author(s):  
Yao-Chi Chuang ◽  
Naoki Yoshimura ◽  
Chao-Cheng Huang ◽  
Po-Hui Chiang ◽  
Michael B. Chancellor

2001 ◽  
Vol 36 (6) ◽  
pp. 630-635 ◽  
Author(s):  
R. Holma ◽  
P. Salmenperä ◽  
J. Lohi ◽  
H. Vapaatalo ◽  
R. Korpela

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