Transition-metal-free nucleophilic 211At-astatination of spirocyclic aryliodonium ylides-Reference-Cited by-同舟云学术

Transition-metal-free nucleophilic 211At-astatination of spirocyclic aryliodonium ylides

Published:2021 Issue: Volume: Page:
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Matsuoka Keitaro¹²³⁴,Obata Honoka¹²³⁴⁵,Nagatsu Kotaro⁵⁶⁷⁸⁴,Kojima Masahiro¹²³⁴,Yoshino Tatsuhiko¹²³⁴^ORCID,Ogawa Mikako¹²³⁴⁹,Matsunaga Shigeki¹²³⁴⁹^ORCID

Affiliation:

1. Faculty of Pharmaceutical Science

2. Hokkaido University

3. Sapporo 060-0812

4. Japan

5. Department of Advanced Nuclear Medicine Sciences

6. Institute for Quantum Medical Science

7. National Institutes for Quantum and Radiological Science and Technology

8. Chiba

9. Global Station for Biosurfaces and Drug Discovery

Abstract

The transition-metal-free nucleophilic ²¹¹At-astatination of aryliodonium ylides, involving those derived from multi-functionalized molecules and heteroarenes, proceeded with good to excellent radiochemical yields.

Funder

Japan Society for the Promotion of Science

Adaptable and Seamless Technology Transfer Program through Target-Driven R and D

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB00789K

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2. Alpha-Emitters and Targeted Alpha Therapy in Oncology: from Basic Science to Clinical Investigations