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Access to C(sp3) borylated and silylated cyclic molecules: hydrogenation of corresponding arenes and heteroarenes.
Chhabra, Arzoo; Reich, Sabrina; Shannon, Timothy M; Maleczka, Robert E; Smith, Milton R.
Afiliação
  • Chhabra A; Department of Chemistry, Michigan State University 578 S Shaw Lane East Lansing Michigan 48824 USA maleczka@chemistry.msu.edu.
  • Reich S; Department of Chemistry, Michigan State University 578 S Shaw Lane East Lansing Michigan 48824 USA maleczka@chemistry.msu.edu.
  • Shannon TM; Department of Chemistry, Michigan State University 578 S Shaw Lane East Lansing Michigan 48824 USA maleczka@chemistry.msu.edu.
  • Maleczka RE; Department of Chemistry, Michigan State University 578 S Shaw Lane East Lansing Michigan 48824 USA maleczka@chemistry.msu.edu.
  • Smith MR; Department of Chemistry, Michigan State University 578 S Shaw Lane East Lansing Michigan 48824 USA maleczka@chemistry.msu.edu.
RSC Adv ; 14(15): 10590-10607, 2024 Mar 26.
Article em En | MEDLINE | ID: mdl-38567346
ABSTRACT
This paper presents a simple and cost-effective hydrogenation method for synthesizing a myriad of cycloalkanes and saturated heterocycles bearing boryl or silyl substituents. The catalyst used are heterogeneous, readily available, bench stable, and recyclable. Also demonstrated is the application of the method to compounds that possess both boryl and silyl groups. When combined with Ir-catalyzed sp2 C-H borylation, such hydrogenations offer a two-step complementary alternative to direct sp3 C-H borylations that can suffer selectivity and reactivity issues. Of practical value to the community, complete stereochemical analyses of reported borylated compounds that were never fully characterized are reported herein.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2024 Tipo de documento: Article
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