TY - JOUR
T1 - Recent Progress in the Synthesis of Deuterated Aldehyde
AU - Shinada, Tetsuro
AU - Nakayama, Atsushi
AU - Okamura, Hironori
AU - Yasuno, Yoko
N1 - Funding Information:
This work was financially supported by JSPS KAKENHI (JP19H04661, JP19H04651, JP20K09396, and JP21K14629), the OCU’s ‘Think globally, act locally’ Research Grant for Young Scientists 2021 through the hometown donation fund of Osaka City, the Uehara Memorial Foundation, and the Sasakawa Scientific Research Grant from The Japan Science Society.
Publisher Copyright:
© 2022 The Chemical Society of Japan.
PY - 2022/10
Y1 - 2022/10
N2 - Deuterium-labeled organic compounds have become indispensable research tools in scientific research. This review focuses on the synthesis of deuterated aldehydes (RCDO) in which the hydrogen at the formyl group is replaced with deuterium. Aldehydes are useful starting materials for organic synthesis. A variety of transformations and derivatizations involving carbon-carbon bond-forming reactions and heteroatom manipulations are possible at the formyl group. Consequently, RCDOs are expected to be a powerful starting material for the synthesis of deuterium-labeled compounds. Many efforts have been devoted to the synthesis of RCDO. The classical and advanced methods are described in this review.
AB - Deuterium-labeled organic compounds have become indispensable research tools in scientific research. This review focuses on the synthesis of deuterated aldehydes (RCDO) in which the hydrogen at the formyl group is replaced with deuterium. Aldehydes are useful starting materials for organic synthesis. A variety of transformations and derivatizations involving carbon-carbon bond-forming reactions and heteroatom manipulations are possible at the formyl group. Consequently, RCDOs are expected to be a powerful starting material for the synthesis of deuterium-labeled compounds. Many efforts have been devoted to the synthesis of RCDO. The classical and advanced methods are described in this review.
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U2 - 10.1246/bcsj.20220202
DO - 10.1246/bcsj.20220202
M3 - Review article
AN - SCOPUS:85141335824
SN - 0009-2673
VL - 95
SP - 1461
EP - 1473
JO - Bulletin of the Chemical Society of Japan
JF - Bulletin of the Chemical Society of Japan
IS - 10
ER -