Lewis Acid-Promoted [2 + 1] Cycloaddition Reactions of a 1-Seleno-2-silylethene to 2-Phosphonoacrylates:  Stereoselective Synthesis of a Novel Functionalized α-Aminocyclopropanephosphonic Acid

1998 ◽  
Vol 63 (17) ◽  
pp. 5919-5928 ◽  
Author(s):  
Shoko Yamazaki ◽  
Takashi Takada ◽  
Tomomi Imanishi ◽  
Yumiko Moriguchi ◽  
Shinichi Yamabe
Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 692
Author(s):  
Víctor E. Macías-Villamizar ◽  
Luís Cuca-Suárez ◽  
Santiago Rodríguez ◽  
Florenci V. González

We report on the regio- and stereoselective synthesis of tetrahydrofurans by reaction between epoxides and alkenes in the presence of a Lewis acid. This is an unprecedented formal [3+2] cycloaddition reaction between an epoxide and an alkene. The chemical reaction represents a very concise synthesis of tetrahydrofurans from accessible starting compounds.


ChemInform ◽  
2003 ◽  
Vol 34 (14) ◽  
Author(s):  
Ana M. Gomez ◽  
Clara Uriel ◽  
Serafin Valverde ◽  
Slawomir Jarosz ◽  
J. Cristobal Lopez

2014 ◽  
Vol 50 (40) ◽  
pp. 5242-5244 ◽  
Author(s):  
Jacob P. MacDonald ◽  
Benjamin H. Shupe ◽  
John D. Schreiber ◽  
Annaliese K. Franz

A Lewis acid-catalyzed stereoselective [3+2] annulation of crotylsilanes with iminooxindoles is reported to access 2,3′-pyrrolidinyl spirooxindoles with four stereocenters.


2018 ◽  
Vol 29 (6) ◽  
pp. 1709-1721 ◽  
Author(s):  
Leila Barama ◽  
Brahim Bayoud ◽  
Fouad Chafaa ◽  
Abdelmalek Khorief Nacereddine ◽  
Abdelhafid Djerourou

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