@article{a891cf68da8f4ce6bb6f09c89a8a9e10,
title = "Ni-Catalyzed Regioselective Reductive 1,3-Dialkenylation of Alkenes",
abstract = "Dicarbofunctionalization is an important efficient synthetic technique for adding two chemical moieties across an alkene. Here, a novel method of reductive dicarbofunctionalization has been developed using a single alkenyl triflate as the electrophile, combined with an unactivated alkene. The reaction does not require an external auxiliary and proceeds with complete regioselectivity.",
author = "Wickham, {Laura M.} and Dhungana, {Roshan K.} and Ramesh Giri",
note = "Funding Information: We gratefully acknowledge the NIH NIGMS (R35GM133438) and The Pennsylvania State University (PSU) for their support of this work. We also thank Dr. Rishi Sapkota for the assistance with the isolation and characterization of compound 8 . We thank Dr. Hemant Yennawar at the Pennsylvania State University for the X-ray crystallographic analysis of compound 2a . The X-ray instrument was funded by the NIH SIG S10 grants (1S10OD028589-01 and 1S10RR023439-01). Publisher Copyright: {\textcopyright} 2022 The Authors. Published by American Chemical Society.",
year = "2022",
doi = "10.1021/acsomega.2c06417",
language = "English (US)",
journal = "ACS Omega",
issn = "2470-1343",
publisher = "American Chemical Society",
}