Literature DB >> 32319503

Dehydration reactions in polyfunctional natural products.

Per Hjerrild1, Thomas Tørring, Thomas B Poulsen.   

Abstract

Covering: up to 2020In this review, we present state of the art methods for performing dehydration reactions in alcohol substrates to deliver alkene products. The dehydration of alcohols typically proceeds through activation of the alcoholic moiety to a nucleofugal species followed by a subsequent elimination step. While the alcohol is a quintessential functional group, selective dehydration of alcohols in complex molecular scaffolds has not been harnessed to allow molecular diversification strategies. We present the perspective of utilizing complex molecular compounds containing alcoholic functionalities to generate novel molecular constructs that impose on chemical space of characterized bioactivity. Nature inspires the direct and selective dehydration of alcohols in complex molecules and demonstrates a potential that has not yet been realized by chemical methodology. We present challenging substrates for direct and selective dehydration reactions and argue that chemical methodology solving the challenges presented will be valued by synthetic and natural product chemists alike.

Entities:  

Year:  2020        PMID: 32319503     DOI: 10.1039/d0np00009d

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  2 in total

1.  Developing Photoaffinity Probes for Dopamine Receptor D2 to Determine Targets of Parkinson's Disease Drugs.

Authors:  Spencer T Kim; Emma J Doukmak; Raymond G Flax; Dylan J Gray; Victoria N Zirimu; Ebbing de Jong; Rachel C Steinhardt
Journal:  ACS Chem Neurosci       Date:  2022-10-02       Impact factor: 5.780

2.  A donor-acceptor complex enables the synthesis of E-olefins from alcohols, amines and carboxylic acids.

Authors:  Kun-Quan Chen; Jie Shen; Zhi-Xiang Wang; Xiang-Yu Chen
Journal:  Chem Sci       Date:  2021-04-05       Impact factor: 9.825

  2 in total

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