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First synthesis, rotamerism and herbicidal evaluation of substituted s-triazines with amino-1,3-dioxane groups

DOI: 10.1515/HC.2006.12.2.151

Source and publish data:

Heterocyclic Communications p. 151 - 156 (2006)

Update date:2022-08-29

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Authors:

Fazekas, MarijanaFazekas, Marijana

Darabantu, MirceaDarabantu, Mircea

Pintea, MonicaPintea, Monica

Lameiras, PedroLameiras, Pedro

Bele, ConstantinBele, Constantin

Berghian, CameliaBerghian, Camelia

Ple, NellyPle, Nelly

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Article abstract of DOI:10.1515/HC.2006.12.2.151

First pure enantiomeric 5-amino-1,3-dioxane, obtained by total diastereospecific ring closure of (1S,2S)-2-amino-1-(4-ni-trophenyl)-1,3- propanediol ("nitrophenylserinol") reacted with cyanuryl chloride to afford N-substituted amino-s-triazines and melami

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Full text of DOI:10.1515/HC.2006.12.2.151

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Brought to you by | Purdue University Libraries  
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Download Date | 5/27/15 7:46 AM  
Brought to you by | Purdue University Libraries  
Authenticated  
Download Date | 5/27/15 7:46 AM  
Brought to you by | Purdue University Libraries  
Authenticated  
Download Date | 5/27/15 7:46 AM  
Brought to you by | Purdue University Libraries  
Authenticated  
Download Date | 5/27/15 7:46 AM  
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Products guided by the article

Product name:2,4-dichloro-6-{[(4S,5S)-4-(4-nitrophenyl)-1,3-dioxan-5-yl]amino}-s-triazine

Cas No:900797-83-3

900797-83-3

R&D Labs maybe for 900797-83-3

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