Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives

Organic Letters

Volumn 17, Issue 13, 2015, Pages 3260-3263

  Han, Jie ^a,b   Hou, Xisen ^a   Ke, Chenfeng ^a   Zhang, Huacheng ^a   Strutt, Nathan L ^a   Stern, Charlotte L ^a   Stoddart, J Fraser ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

^b NANKAI UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84935049339     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/acs.orglett.5b01418     Document Type: Article

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57. In principle, increasing the reaction time should increase the production of deprotected derivatives of P5. In our experiments, we noticed that increasing the amount of deprotecting agent can also lead to an increase in the yields of products in shorter reaction times.
58. The methylene protons in the labeled structures for the NMR spectra in Figure 1 are diastereotopic, but they are grouped together with one label. They are most likely exchanging rapidly on the NMR time scale; however, they are not equivalent as suggested by the label.