PENG HU, Karsten Berning, Yun-Wah Lam, Isabel Hei-Ma NG, Chi-Chung YEUNG, Michael Hon-Wah Lam, Development of a Visible Light Triggerable Traceless Staudinger Ligation Reagent, The Journal of Organic Chemistry, 10.1021/acs.joc.8b01370, (2018).
Traceless Electrophilic Amination for the Synthesis of Unprotected Cyclic β-Amino Acids Jin-Sheng Yu, Miguel Espinosa, Hidetoshi Noda*, Masakatsu Shibasaki* *Institute of Microbial Chemistry (BIKAKEN), Tokyo, 3-14-23 Kamiosaki, Shinagawa-ku, Tokyo 141-0021, … Traceless Protection for More Broadly Applicable Olefin Traceless Protection for More Broadly Applicable Olefin Metathesis. Yucheng Mu. Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, MA, 02467 USA. These authors contributed equally to this work. Search for more papers by this author. Thach T. Nguyen. Traceless Directing Group Assisted Cobalt‐Catalyzed C−H
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Corresponding Author. E-mail address: sliu@ustc.edu.cn CAS Key Laboratory of Soft Matter Chemistry, Hefei National Laboratory for Physical, Sciences at the Microscale, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui 230026 (China)
Traceless native chemical ligation of lipid-modified Jun 03, 2020 Traceless Staudinger Ligation | Sigma-Aldrich Among the suitable phosphine reagents for traceless Staudinger ligations, diphenylphosphinemethanethiol (Figure 1), developed by Raines and co-workers, exhibits the best reactivity profile and has already found widespread application. This Raines ligation reagent is first acylated. Treatment with an azide leads to the formation of an aza-ylide. N 2 H 4 as traceless mediator for homo- and cross- aryl Nov 09, 2018 A Traceless Directing Group for CH Borylation - Chemistry