Site-Selective and Enantioselective C-H Functionalization of Unactivated C–H Bonds in the Presence of Nitrogen Functionality Öffentlichkeit

Cai, Qinyan (Spring 2022)

Permanent URL: https://etd.library.emory.edu/concern/etds/gt54kp343?locale=de
Published

Abstract

The rhodium-catalyzed C-H functionalization of unactivated C-H bonds by means of donor/acceptor carbene-induced C-H functionalization was extended to substrates containing nitrogen functionality. The optimum nitrogen protecting group was the phthalimido group and aryldiazoacetates were used as the precursors to the donor/acceptor carbenes. By using Rh2(S-2-Cl-5-BrTPCP)4 as catalyst, selective C-H functionalization occurred at the most sterically accessible methylene site, whereas the desymmetrization of cyclopentylamine and cyclohexylamine derivatives was possible when Rh2(S-TPPTTL)4 was used as a catalyst.

Table of Contents

Table of Contents

Site-selective and Enantioselective C-H Functionalization of Unactivated C-H Bonds in the Presence of Amine Functionalities………………………………………………………….…...1

1 Introduction………………………………………...………………………………….……….1

2 Results and Discussion…………………………......………………………………….……….4

2.1 The Discovery of Protecting Groups………………..……………………………….4

2.2 The Study about the Distance from the Primary Amines……………..………..…13

2.3 Expansion of the Scope to Tertiary Sites……………………………………..….…17

2.4 Further Support of Asymmetric Induction………………………..………………22

2.5 Desymmetrization of Cyclic Systems……………………………………………....27

2.6 Reaction Scope with Aryldiazoacetates………………………………..…..………31

3 Conclusions and Future Directions……………......………………………………….…..….32

4 Experimental Part…………………….………………………………………………………33

4.1 General Procedures for Substrates and C-H Insertion Products……...…..……...33

4.2 Experimental Part for Substrates….………...………...…………………………...36

4.4 Experimental Part for Aryldiazoacetate……............……………………………...42

4.5 Experimental Part for C-H Insertion Products.........……………………………...43

Reference………………………………………………………………………………………..54

About this Honors Thesis

Rights statement
  • Permission granted by the author to include this thesis or dissertation in this repository. All rights reserved by the author. Please contact the author for information regarding the reproduction and use of this thesis or dissertation.
School
Department
Degree
Submission
Language
  • English
Research Field
Stichwort
Committee Chair / Thesis Advisor
Committee Members
Zuletzt geändert

Primary PDF

Supplemental Files