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Developing Pd(II) Catalyzed Double sp<sup>3</sup> C–H Alkoxylation for Synthesis of Symmetric and Unsymmetric Acetals
Abstract
An effective Pd(II) catalyzed double unactivated C(sp<sup>3</sup>)–H alkoxylation has been developed to prepare both symmetric and unsymmetric acetals. This new reaction demonstrates good functional group tolerance, excellent reactivity, and high yields. A variety of novel acetals can be readily accessed via this new method- Text
- Journal contribution
- Biochemistry
- Genetics
- Molecular Biology
- Developmental Biology
- Environmental Sciences not elsewhere classified
- Biological Sciences not elsewhere classified
- Chemical Sciences not elsewhere classified
- Symmetric
- Pd
- Unsymmetric AcetalsAn
- variety
- unsymmetric acetals
- method
- Synthesi
- novel acetals
- Alkoxylation
- Catalyzed
- unactivated
- group tolerance
- sp
- yield
- alkoxylation
- reactivity
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Last time updated on 12/02/2018
This paper was published in The Francis Crick Institute.
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