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- N-Insertion reaction mechanisms of phenyl azides with a hafnium hydride complex: a quantum chemistry calculation. Hujun Xie, Lihong Wang, Yang Li, Jian Kuang, Zunyi Wu, Ting Fan, Qunfang Lei, Wenjun Fang
, New J. Chem.
, 2017
, 41
, 5007
- Synthesis of radiolabelled aryl azides from diazonium salts: experimental and computational results permit the identification of the preferred mechanism. Sameer M. Joshi, Abel de Cózar, Vanessa Gómez-Vallejo, Jacek Koziorowski, Jordi Llop, Fernando P. Cossío
, Chem. Commun.
, 2015
, 51
, 8954
- Mechanism and selectivity for zinc-mediated cycloaddition of azides with alkynes: a computational study. Yingzi Li, Xiaotian Qi, Yu Lei, Yu Lan
, RSC Adv.
, 2015
, 5
, 49802
- Why is phenyl azide so unreactive in [3 + 2] cycloaddition reactions? Demystifying Sustmann's paradigmatic parabola. Luis R. Domingo, Mar Ríos-Gutiérrez, Patricia Pérez
, Org. Chem. Front.
, 2023
, 10
, 5579
- The reaction of ortho-substituted aromatic azides with boron trichloride or trifluoride. Piero Spagnolo, Paolo Zanirato
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 2615
- Unravelling the strain-promoted [3+2] cycloaddition reactions of phenyl azide with cycloalkynes from the molecular electron density theory perspective. Luis R. Domingo, Nivedita Acharjee
, New J. Chem.
, 2020
, 44
, 13633
- Enabling the formation of native mAb, Fab′ and Fc-conjugates using a bis-disulfide bridging reagent to achieve tunable payload-to-antibody ratios (PARs). Fabien Thoreau, Léa N. C. Rochet, James R. Baker, Vijay Chudasama
, Chem. Sci.
, 2023
, 14
, 3752
- A mechanistic insight into the effect of piperidine as an organocatalyst on the [3 + 2] cycloaddition reaction of benzalacetone with phenyl azide from a computational study. J. Tajabadi, M. Bakavoli, M. Gholizadeh, H. Eshghi
, Org. Biomol. Chem.
, 2016
, 14
, 7324
- Copper fluorapatite assisted synthesis of new 1,2,3-triazoles bearing a benzothiazolyl moiety and their antibacterial and anticancer activities. Sambhaji T. Dhumal, Amarsinh R. Deshmukh, Kiran R. Kharat, Bhaskar R. Sathe, Santosh S. Chavan, Ramrao A. Mane
, New J. Chem.
, 2019
, 43
, 7663
- An efficient cyclization of lapachol to new benzo[h]chromene hybrid compounds: a stepwise vs. one-pot esterification-click (CuAAC) study. Alexander F. de la Torre, Akbar Ali, Bernhard Westermann, Guillermo Schmeda-Hirschmann, Mariano Walter Pertino
, New J. Chem.
, 2018
, 42
, 19591