Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/159960
Title: Intramolecular alkene-alkene coupling via Rh(III)-catalyzed alkenyl sp² C-H functionalization: divergent pathways to indene or α-naphthol derivatives
Authors: Maraswami, Manikantha
Diggins, Thomas
Goh, Jeffrey
Tio, Raymond
Ong, Renee Wan Qing
Hirao, Hajime
Loh, Teck-Peng
Keywords: Science::Chemistry
Issue Date: 2021
Source: Maraswami, M., Diggins, T., Goh, J., Tio, R., Ong, R. W. Q., Hirao, H. & Loh, T. (2021). Intramolecular alkene-alkene coupling via Rh(III)-catalyzed alkenyl sp² C-H functionalization: divergent pathways to indene or α-naphthol derivatives. ACS Catalysis, 11(18), 11494-11500. https://dx.doi.org/10.1021/acscatal.1c03175
Project: RG12/18-S
Journal: ACS Catalysis
Abstract: Highly selective synthesis of either indene or 1-naphthol derivatives through intramolecular alkene-alkene cross-coupling is reported. The reaction works with different alkene pairs that couple to give the corresponding products in good to satisfactory yields. The indene products of our reaction also allow further derivatization. The reaction pathway is dependent on alkene functionalities.
URI: https://hdl.handle.net/10356/159960
ISSN: 2155-5435
DOI: 10.1021/acscatal.1c03175
Schools: School of Physical and Mathematical Sciences 
Rights: © 2021 American Chemical Society. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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