ChemInform Abstract: Unusual Mechanistic Pathway for the Synthesis of Novel Spiro-oxindoles via 3-Phenyl-5-isoxazolone Ring Cleavage by Secondary Amino Acids.

ChemInform ◽  
2011 ◽  
Vol 42 (43) ◽  
pp. no-no
Author(s):  
Neelakandan Vidhya Lakshmi ◽  
Yuvaraj Arun ◽  
Paramasivam T. Perumal

2011 ◽  
Vol 52 (27) ◽  
pp. 3437-3442 ◽  
Author(s):  
Neelakandan Vidhya Lakshmi ◽  
Yuvaraj Arun ◽  
Paramasivam T. Perumal


ChemInform ◽  
2010 ◽  
Vol 30 (21) ◽  
pp. no-no
Author(s):  
Roberto Ballini ◽  
Fabrizio Papa ◽  
Corrado Abate
Keyword(s):  






2013 ◽  
Vol 54 (14) ◽  
pp. 1817-1820 ◽  
Author(s):  
Neelakandan Vidhya Lakshmi ◽  
Paramasivan T. Perumal


1978 ◽  
Vol 33 (10) ◽  
pp. 1145-1149 ◽  
Author(s):  
Nazmi Kassab ◽  
Abdul Harhash ◽  
Said Elbahaii

Abstract The oxazoline ring in 4-arylazo-2-aryl-2-oxazolin-5-ones (1) is converted to triazolyl-carbonyl amino acids 2, 4 and 6 by the nucleophiles glycine, anthranilic and p-aminobenzoic acids, respectively. The arylidene derivatives 3 of 2-triazolyl-2-oxazolin-5-one were obtained. Triazolylbenzoxazinones 5, were obtained by the ring closure of the amino acid 4.Grignard's reagent effected ring cleavage of the oxazolinone ring in 4-cinnamylidene-2-aryl-2-oxazolin-5-ones yielding the carbinols 8, the latter cyclizes either in acidic or alkaline medium to afford either benzotropilidenes or oxazolines, respectively.



2011 ◽  
Vol 49 (2) ◽  
pp. 118-123 ◽  
Author(s):  
S. M. Buha ◽  
A. Panchal ◽  
H. Panchal ◽  
R. Chambhare ◽  
P. R. Patel ◽  
...  


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