DABCO-catalysed highly diastereoselective synthesis of 1,3-indandione containing fully saturated spirocyclopentanes involving 2-(2′-ketoalkyl)-1,3-indandiones and nitrostyrenes

Highly functionalized 1,3-indandione containing spirocyclopentanes has been synthesized by reacting nitrostyrenes with 2-(2'-ketoalkyl)-1,3-indandiones using a catalytic amount of DABCO. The resultant products possess three consecutive chiral centres in addition to a spirocyclic centre and are obtained in a highly diastereoselective manner using a catalytic amount of the organic base, DABCO.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra04224k
Citations
1
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
0.94

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article

DABCO-catalysed highly diastereoselective synthesis of 1,3-indandione containing fully saturated spirocyclopentanes involving 2-(2′-ketoalkyl)-1,3-indandiones and nitrostyrenes

Barla Thirupathi, Kamrul Islam, Gitanjali Mishra, Arundhuti Chakraborty et al.
1 citations
RSC Advances
Asymmetric Synthesis and Catalysis
0.94
article

DABCO-catalysed highly diastereoselective synthesis of 1,3-indandione containing fully saturated spirocyclopentanes involving 2-(2′-ketoalkyl)-1,3-indandiones and nitrostyrenes

Barla Thirupathi, Kamrul Islam, Gitanjali Mishra, Arundhuti Chakraborty, Missa Saril Bobonga
article en
1 citations

Abstract

Highly functionalized 1,3-indandione containing spirocyclopentanes has been synthesized by reacting nitrostyrenes with 2-(2'-ketoalkyl)-1,3-indandiones using a catalytic amount of DABCO. The resultant products possess three consecutive chiral centres in addition to a spirocyclic centre and are obtained in a highly diastereoselective manner using a catalytic amount of the organic base, DABCO.

RSC AdvancesVol. 15(37)
Indian Institute of Science Education and Research Berhampur (IN)
Department of Science and Technology, Ministry of Science and Technology, India, Indian Institute of Science Education and Research Mohali, Science and Engineering Research Board
Openalex Percentile: Top 22%
Asymmetric Synthesis and Catalysis
0.94
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