Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774456
Title: Lithiation-borylation methodology : applications in the synthesis of polypropionate fragment and polyfluoromethylation reactions of organoboronic esters
Author: Zhou, Bin
ISNI:       0000 0004 7961 6608
Awarding Body: University of Bristol
Current Institution: University of Bristol
Date of Award: 2019
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
The thesis describes the applications of lithiation-borylation methodology in polypropionate synthesis and the synthesis of organofluorine compounds. Firstly, an efficient method for the synthesis of polypropionate fragments based on building block assembly strategy using lithiation-borylation reaction has been developed. Benzoate ester 302 can react with boronic ester 347 efficiently via lithiationborylation reaction and subsequent oxidation to afford alcohol 353 in good yield and with excellent diastereoselectivity, which can be applied in the synthesis of polypropionate fragment 358, a key intermediate of 6-deoxyerythronolide. Some limitations, such as substrate control and O-migration, were observed in the reaction process. Secondly, we extensively explored the introduction of difluoromethyl and monofluoromethyl groups by lithiation-borylation reaction with organoboronic esters. The difluoromethylation and monofluoromethylation reactions proved to be very challenging due to the instability of in situ generated fluorinated carbanion 417 or 423. Generally, the formation of boronate complex 419 or 424 was not detected. Additionally, we proposed some other strategies for the future work.
Supervisor: Aggarwal, Varinder ; Willis, Chris Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.774456  DOI: Not available
Share: