α‐Cyclodextrin Encapsulation of Bicyclo[1.1.1]pentane Derivatives: A Storable Feedstock for Preparation of [1.1.1]Propellane-Reference-Cited by-同舟云学术

α‐Cyclodextrin Encapsulation of Bicyclo[1.1.1]pentane Derivatives: A Storable Feedstock for Preparation of [1.1.1]Propellane

Published:2021-01-04 Issue:5 Volume:60 Page:2578-2582
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Matsunaga Tadafumi¹,Kanazawa Junichiro¹^ORCID,Ichikawa Tomohiro¹,Harada Mei¹,Nishiyama Yusuke²³^ORCID,Duong Nghia Tuan²^ORCID,Matsumoto Takashi⁴,Miyamoto Kazunori¹^ORCID,Uchiyama Masanobu¹⁵⁶^ORCID

Affiliation:

1. Graduate School of Pharmaceutical Sciences The University of Tokyo 7-3-1 Hongo, Bunkyo-ku Tokyo 113-0033 Japan

2. RIKEN-JEOL Collaboration Center and SPring-8 Center RIKEN, Tsurumi Yokohama Kanagawa 230-0045 Japan

3. JEOL RESONANCE Inc. 3-1-2 Musashino, Akishima Tokyo 196-8558 Japan

4. Rigaku Corporation 3-9-12 Matsubara-cho, Akishima Tokyo 196-8666 Japan

5. Cluster for Pioneering Research (CPR) RIKEN 2-1 Hirosawa, Wako-shi Saitama 351-0198 Japan

6. Research Initiative for Supra-Materials (RISM) Shinshu University 3-15-1 Tokida, Ueda Nagano 386-8567 Japan

Funder

Japan Society for the Promotion of Science

Core Research for Evolutional Science and Technology

Nagase Science Technology Foundation

Sumitomo Foundation

Uehara Memorial Foundation

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202014997

Reference50 articles.

2. 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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4. Investigation of a Bicyclo[1.1.1]pentane as a Phenyl Replacement within an LpPLA2 Inhibitor

5. Toward Resolving the Resveratrol Conundrum: Synthesis and in Vivo Pharmacokinetic Evaluation of BCP–Resveratrol

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