ChemInform Abstract: Nucleophilic Ring Opening of Aziridine-2-carboxylates with Wittig Reagents. An Enantioefficient Synthesis of Unsaturated Amino Acids.

ChemInform ◽  
1987 ◽  
Vol 18 (32) ◽  
Author(s):  
J. E. BALDWIN ◽  
R. M. ADLINGTON ◽  
N. G. ROBINSON
ChemInform ◽  
2010 ◽  
Vol 33 (4) ◽  
pp. no-no
Author(s):  
Jaume Farras ◽  
Xavier Ginesta ◽  
Peter W. Sutton ◽  
Joan Taltavull ◽  
Frank Egeler ◽  
...  

Tetrahedron ◽  
2001 ◽  
Vol 57 (36) ◽  
pp. 7665-7674 ◽  
Author(s):  
Jaume Farràs ◽  
Xavier Ginesta ◽  
Peter W Sutton ◽  
Joan Taltavull ◽  
Frank Egeler ◽  
...  

ACS Omega ◽  
2018 ◽  
Vol 3 (12) ◽  
pp. 17562-17572 ◽  
Author(s):  
Gaurav Goswami ◽  
Navya Chauhan ◽  
Abhijit Mal ◽  
Subhomoy Das ◽  
Mowpriya Das ◽  
...  

Molbank ◽  
10.3390/m1199 ◽  
2021 ◽  
Vol 2021 (2) ◽  
pp. M1199
Author(s):  
Milene A. G. Fortunato ◽  
Filipa Siopa ◽  
Carlos A. M. Afonso

Using environmentally friendly conditions, the nucleophilic ring-opening reaction of 6-azabicyclo[3.1.0]hex-3-en-2-ol with 1-methyl-1H-tetrazole-5-thiol provided a novel thiol-incorporated aminocyclopentitol, (1R,4S,5S)-5-((3-hydroxypropyl)amino)-4-((1-methyl-1H-tetrazol-5-yl)thio)cyclopent-2-en-1-ol, in excellent yield (95%). The newly synthesized compound was analyzed and characterized via 1H, 13C-NMR, HSQC, and mass spectral data.


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