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Julius Rebek

Showing results (111-120 of 241) with videos related to

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Chemical Communications (Cambridge, England)|August 16, 2005
Lower rim mono-functionalization of resorcinarenesFrank Hauke, Andrew J Myles, Julius Rebek
Chemical Communications (Cambridge, England)|March 9, 2019
Cyclizations catalyzed inside a hexameric resorcinarene capsuleYujie Zhu, Julius Rebek Jr, Yang Yu
Journal of the American Chemical Society|March 21, 2002
Water-stabilized cavitandsAdel Rafai Far, Alexander Shivanyuk, Julius Rebek
Science (New York, N.Y.)|July 28, 2007
Stabilization of labile carbonyl addition intermediates by a synthetic receptorTetsuo Iwasawa, Richard J Hooley, Julius Rebek
Chemical Communications (Cambridge, England)|January 4, 2003
Resorcin[6]arene as a building block for tubular crystalline state architecturesByron W Purse, Alexander Shivanyuk, Julius Rebek
Journal of the American Chemical Society|December 4, 2003
Reactivity and molecular recognition: amine methylation by an introverted esterByron W Purse, Pablo Ballester, Julius Rebek
Journal of the American Chemical Society|January 28, 2021
Selective Macrocycle Formation in CavitandsJi-Min Yang, Yang Yu, Julius Rebek
Journal of the American Chemical Society|November 17, 2007
Detection of reactive tetrahedral intermediates in a deep cavitand with an introverted functionalityRichard J Hooley, Tetsuo Iwasawa, Julius Rebek
Chemical Communications (Cambridge, England)|December 3, 2008
A cavitand with a fluorous rim acts as an amine receptorRichard J Hooley, Per Restorp, Julius Rebek
Journal of the American Chemical Society|August 11, 2005
A deep cavitand provides a structured environment for the Menschutkin reactionByron W Purse, Arnaud Gissot, Julius Rebek
Pageof 25

Showing results (111-120 of 241) with videos related to

Sort By:
Pageof 25
Chemical Communications (Cambridge, England)|August 16, 2005
Lower rim mono-functionalization of resorcinarenesFrank Hauke, Andrew J Myles, Julius Rebek
Chemical Communications (Cambridge, England)|March 9, 2019
Cyclizations catalyzed inside a hexameric resorcinarene capsuleYujie Zhu, Julius Rebek Jr, Yang Yu
Journal of the American Chemical Society|March 21, 2002
Water-stabilized cavitandsAdel Rafai Far, Alexander Shivanyuk, Julius Rebek
Science (New York, N.Y.)|July 28, 2007
Stabilization of labile carbonyl addition intermediates by a synthetic receptorTetsuo Iwasawa, Richard J Hooley, Julius Rebek
Chemical Communications (Cambridge, England)|January 4, 2003
Resorcin[6]arene as a building block for tubular crystalline state architecturesByron W Purse, Alexander Shivanyuk, Julius Rebek
Journal of the American Chemical Society|December 4, 2003
Reactivity and molecular recognition: amine methylation by an introverted esterByron W Purse, Pablo Ballester, Julius Rebek
Journal of the American Chemical Society|January 28, 2021
Selective Macrocycle Formation in CavitandsJi-Min Yang, Yang Yu, Julius Rebek
Journal of the American Chemical Society|November 17, 2007
Detection of reactive tetrahedral intermediates in a deep cavitand with an introverted functionalityRichard J Hooley, Tetsuo Iwasawa, Julius Rebek
Chemical Communications (Cambridge, England)|December 3, 2008
A cavitand with a fluorous rim acts as an amine receptorRichard J Hooley, Per Restorp, Julius Rebek
Journal of the American Chemical Society|August 11, 2005
A deep cavitand provides a structured environment for the Menschutkin reactionByron W Purse, Arnaud Gissot, Julius Rebek
Pageof 25