Organophotocatalyzed C‐Si Bond Fragmentation Using Silyl Ethers as Radical Precursors DOI Creative Commons
Adrián Luguera Ruiz,

Valentina Benazzi,

Federico Tucci

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2024, Номер 366(19), С. 4132 - 4138

Опубликована: Июль 19, 2024

Abstract In this work, silyl ethers of phenols and alcohols have been successfully prepared tested as neutral carbon (silicon) centered radical precursors. The organophotocatalyzed oxidation (by the Fukuzumi catalyst) these caused cleavage a C−Si (or Si−Si) bond for release desired to be used forging C( sp 3 ) −C( −Si) bonds via Giese reaction.

Язык: Английский

Electrochemistry-Enabled C-Heteroatom Bond Formation of Alkyl Germanes DOI

Markus D. Schoetz,

Kristina Deckers,

Gurdeep Singh

и другие.

Journal of the American Chemical Society, Год журнала: 2024, Номер 146(31), С. 21257 - 21263

Опубликована: Июль 26, 2024

Because of their robustness and orthogonal reactivity features, alkyl germanes bear significant potential as functional handles for the construction C(sp3)-rich scaffolds, especially in context modular synthetic approaches. However, to date, only radical-based has been accessible from these handles, which limits types possible decorations. Here, we describe first general C(sp3)–heteroatom bond formation (−GeEt3) by leveraging electrochemistry unlock polar reactivity. This approach allowed us couple C(sp3)–GeEt3 with a variety nucleophiles construct ethers, esters, amines, amides, sulfonamides, sulfides, well C–P, C–F, C–C bonds. The compatibility electrochemical strategy C1 motif was also showcased, involving sequential functionalization Cl, Bpin, ultimately GeEt3 via electrochemistry.

Язык: Английский

Процитировано

4

Developments in the synthesis of allylsilanes by transition metal–catalyzed silylation of 1,3-dienes with disilanes DOI
Nobuki Katayama, Yasushi Obora

Chemistry Letters, Год журнала: 2024, Номер 53(7)

Опубликована: Июль 1, 2024

Abstract This highlight review overviews developments in the synthesis of allylsilanes by transition metal–catalyzed silylation 1,3-dienes with disilanes. We specifically disilylation, which installs 2 silicon atoms, and silyl-functionalization, both another atom using disilanes reagents such as nucleophiles electrophiles. Utilizing these methods for provides a robust protocol efficient desired 1 step, thereby streamlining silyl-functionalization 1,3-dienes.

Язык: Английский

Процитировано

1

Organophotocatalyzed C‐Si Bond Fragmentation Using Silyl Ethers as Radical Precursors DOI Creative Commons
Adrián Luguera Ruiz,

Valentina Benazzi,

Federico Tucci

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2024, Номер 366(19), С. 4132 - 4138

Опубликована: Июль 19, 2024

Abstract In this work, silyl ethers of phenols and alcohols have been successfully prepared tested as neutral carbon (silicon) centered radical precursors. The organophotocatalyzed oxidation (by the Fukuzumi catalyst) these caused cleavage a C−Si (or Si−Si) bond for release desired to be used forging C( sp 3 ) −C( −Si) bonds via Giese reaction.

Язык: Английский

Процитировано

0