Hiroshige OGAWA
@hiroshige_ogawa
Hong Kong University Science and Technology/PhD candidate/Hugh Nakamura lab/Keio MS/Chida-Sato lab
ID: 2853859572
13-10-2014 04:48:29
736 Tweet
259 Followers
420 Following
We are excited to announce that our latest work on the photoinduced nickel catalysis has been accepted in Org. Lett. J Org Chem/Org Lett 🔥 奥くん、佐伯くん、土井さんの論文がOrg. Lett.誌に公開されました！ 岡山大学 Naoki Oku Ken Yamazaki pubs.acs.org/doi/10.1021/ac…
Concise #TotalSyntheses of Leuconoxine-Type Alkaloids Enabled by Palladium/Norbornene-Catalyzed Pyrrole Difunctionalization by Xin Liu (Xin Liu), Yun Zhou, Yu Meng, Qi Zhu, Renhe Li, and Guangbin Dong The Dong Lab at UChicago Chemistry in Angewandte Chemie onlinelibrary.wiley.com/doi/abs/10.100…
Join us today for another incredible total synthesis talk!! This week: Atroposelective Total Synthesis of Lapparbin with Hiroshige Ogawa Link: youtu.be/tjn_gLme8dE Thanks to Kathleen for hosting/editing!! Angewandte Chemie doi.org/10.1002/anie.2…
Convergent #TotalSynthesis of (−)-Calidoustene by Weidong Yao, Ziqi Liu, Hao Ling, Hongyu Wang, Hufeng Zheng, Shao-Hua Wang, Dao-Yong Zhu, Sheng-Yong Zhang, and Xiaoming Chen in J. Am. Chem. Soc. pubs.acs.org/doi/10.1021/ja…
Skeletal Editing Strategies Driven by #TotalSynthesis by Sojung F. Kim, Charis Amber, G. Logan Bartholomew, and Richmond Sarpong Sarpong Group at College of Chemistry in Accounts of Chemical Research ACS Publications pubs.acs.org/doi/10.1021/ac…
Concise #TotalSynthesis of Ambiguine P by Yifan Fei, Bo Fan, Zhigang Liu, Mengyu Ba, Zhongwen Cui, Peng Yang, and Ang Li at Shanghai Institute of Organic Chemistry in J. Am. Chem. Soc. pubs.acs.org/doi/10.1021/ja…
Radicals, tamed! Our new J. Am. Chem. Soc. paper reveals an in situ doublet-state photocatalyst rivaling top photoreductants—enabling borylations & more. Huge congrats to the team! 🎉 #photocatalysis Bristol Chemistry pubs.acs.org/doi/10.1021/ja…
Nucleophilic substitution at a neopentyl-like electrophile ⁉️ Our new, bench-stable, bifunctional Iodo-BCP-TT reagent makes it possible! Our new, highly modular platform to access a broad range of BCP isosteres is now out in Nature Synthesis! ⬇️⬇️⬇️ nature.com/articles/s4416…
Iridium-Catalyzed Nitrene-Mediated Enantioselective 1,2-Hydride Shift Enabled by Attractive Noncovalent Interactions for Chiral δ-Lactam Synthesis | Journal of the American Chemical Society Total Synthesis and Methodology Highlights pubs.acs.org/doi/10.1021/ja…
