Twofold Radical-Based Synthesis of N,C-Difunctionalized Bicyclo[1.1.1]pentanes-Reference-Cited by-同舟云学术

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Twofold Radical-Based Synthesis of N,C-Difunctionalized Bicyclo[1.1.1]pentanes

Published:2021-06-23 Issue:26 Volume:143 Page:9729-9736
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Pickford Helena D.¹,Nugent Jeremy¹,Owen Benjamin¹,Mousseau James. J.²,Smith Russell C.³,Anderson Edward A.¹^ORCID

Affiliation:

1. Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA, United Kingdom

2. Pfizer Worldwide Research and Development, Eastern Point Road, Groton, Connecticut 06340, United States

3. Janssen PRD, 3210 Merryfield Row, San Diego, California 92121, United States

Funder

Engineering and Physical Sciences Research Council

Horizon 2020 Framework Programme

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.1c04180

Reference60 articles.

1. Selected Topics in the Syntheses of Bicyclo[1.1.1]Pentane (BCP) Analogues

2. Recent Advances in the Synthetic Chemistry of Bicyclo[1.1.1]pentane

3. Saturated bioisosteres of benzene: where to go next?

4. Nonconjugated Hydrocarbons as Rigid‐Linear Motifs: Isosteres for Material Sciences and Bioorganic and Medicinal Chemistry

5. Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor

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5. Intermolecular Formal [2π + 2σ] Cycloaddition of Enol Silyl Ethers with Bicyclo[1.1.0]butanes Promoted by Lewis Acids;Organic Letters;2024-07-23

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