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Highly Diastereoselective Hydrosilane‐Assisted Rhodium‐Catalyzed Spiro‐Type Cycloisomerization of Succinimide and Pyrazolone‐Based Functional 1,6‐Dienes
Author(s) -
Li HuiLin,
Huang WeiSheng,
Ling FangYing,
Li Li,
Yan JunHao,
Xu Hao,
Xu LiWen
Publication year - 2021
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.202100372
Subject(s) - cycloisomerization , chemistry , rhodium , succinimide , organosilicon , diastereomer , reagent , catalysis , organic chemistry , intramolecular force , combinatorial chemistry , medicinal chemistry , stereochemistry
Organosilicon compounds are important reagents and synthetic intermediates that play a key role in the construction of new materials and complex products. Here we show a highly diastereoselective rhodium‐catalyzed cycloisomerization of 1,6‐dienes, in which the use of (EtO) 3 SiH accelerates the intramolecular cyclization reaction to afford a novel spiro‐fused succinimide and pyrazolone derivatives in moderate to excellent yields as a single diastereoisomer. The proposed mechanism involves an active Rh−H species from the hydrosilane that is the H‐donor in this spiro‐type cycloisomerization reaction.