Diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and C-acylated chromone adducts via allylic phosphorus ylides

Durga Prasad Gurram; Gangababu Marri; Naveen Jothimani; Yi Ru Chen; Wenwei Lin

doi:10.1039/d4cc03210a

Diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and C-acylated chromone adducts via allylic phosphorus ylides

Durga Prasad Gurram
, Gangababu Marri
, Naveen Jothimani
, Yi Ru Chen
, Wenwei Lin^*

^*Corresponding author for this work

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

3 Citations (Scopus)

Abstract

An organophosphine-controlled diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and C-acylated 2-((chromone-3-yl)methylene)-indandiones is reported. Key attributes of the methodology are the in situ generation of an allylic P-ylide and subsequent regio- and chemoselective intramolecular cyclization reactions that preferentially result in the aforementioned chromone adducts.

Original language	English
Pages (from-to)	9817-9820
Number of pages	4
Journal	Chemical Communications
Volume	60
Issue number	72
DOIs	https://doi.org/10.1039/d4cc03210a
Publication status	Published - 2024 Aug 9

ASJC Scopus subject areas

Electronic, Optical and Magnetic Materials
Catalysis
Ceramics and Composites
General Chemistry
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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10.1039/d4cc03210a

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title = "Diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and C-acylated chromone adducts via allylic phosphorus ylides",

abstract = "An organophosphine-controlled diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and C-acylated 2-((chromone-3-yl)methylene)-indandiones is reported. Key attributes of the methodology are the in situ generation of an allylic P-ylide and subsequent regio- and chemoselective intramolecular cyclization reactions that preferentially result in the aforementioned chromone adducts.",

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T1 - Diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and C-acylated chromone adducts via allylic phosphorus ylides

AU - Gurram, Durga Prasad

AU - Marri, Gangababu

AU - Jothimani, Naveen

AU - Chen, Yi Ru

AU - Lin, Wenwei

PY - 2024/8/9

Y1 - 2024/8/9

N2 - An organophosphine-controlled diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and C-acylated 2-((chromone-3-yl)methylene)-indandiones is reported. Key attributes of the methodology are the in situ generation of an allylic P-ylide and subsequent regio- and chemoselective intramolecular cyclization reactions that preferentially result in the aforementioned chromone adducts.

AB - An organophosphine-controlled diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and C-acylated 2-((chromone-3-yl)methylene)-indandiones is reported. Key attributes of the methodology are the in situ generation of an allylic P-ylide and subsequent regio- and chemoselective intramolecular cyclization reactions that preferentially result in the aforementioned chromone adducts.

UR - https://www.scopus.com/pages/publications/85201776965

UR - https://www.scopus.com/pages/publications/85201776965#tab=citedBy

U2 - 10.1039/d4cc03210a

DO - 10.1039/d4cc03210a

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AN - SCOPUS:85201776965

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JO - Chemical Communications

JF - Chemical Communications

IS - 72

ER -

Diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and C-acylated chromone adducts via allylic phosphorus ylides

Abstract

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