PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
September 19, 2025Chinese Journal of Chemistry13 citations

Iron‐Catalyzed Enantioselective Hydrosilylation of α‐Substituted Vinylsilanes†

View Full Paper
LWLingtao WangMLMinghua LiHYHong-Mei Yan

Key Points

  • The reaction yields high regio- and enantioselectivity, enabling efficient synthesis of chiral vicinal bis(silane)s.
  • Utilizing a localized steric bulky effect in the ligand enhances the overall yield and enantioselectivity significantly.
  • Chiral vicinal bis(silane)s can be synthesized on a gram scale, allowing for practical applications in diverse chemical contexts.
  • Derivatizations of these bis(silane)s lead to high-value products, such as cyclosiloxane and siloxane derivatives.

Abstract

Comprehensive Summary The first iron‐catalyzed asymmetric hydrosilylation of α‐substituted vinylsilanes is reported. This reaction proceeds with high regio‐ and enantioselectivity, providing an efficient access to enantioenriched chiral vicinal bis(silane)s bearing derivatizable Si–H bonds. Importantly, the localized steric bulky effect in the new designed ligand significantly enhances both yield and enantioselectivity. Furthermore, gram‐scale synthesis could be performed smoothly. The derivatizations of the resulting chiral vicinal bis(silane)s are also demonstrated, furnishing high‐value cyclosiloxane and siloxane.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Wang et al. (2025) studied this question.

synapsesocial.com/papers/68d466af31b076d99fa65182https://doi.org/10.1002/cjoc.70268
Ask AI
Helpful
Bookmark
Share
View Full Paper