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Synthesis of γ-aminobutyric acid analogues of restricted conformation. Part 2. The 2-(aminomethyl)cycloalkanecarboxylic acids . Peter D. Kennewell, Saroop S. Matharu, John B. Taylor, Robert Westwood, Peter G. Sammes
, J. Chem. Soc., Perkin Trans. 1
, 1982
, 2563
Adventures in co-crystal land: high Z ′, stoichiometric variations, polymorphism and phase transitions in the co-crystals of four liquid and solid cyclic carboxylic acids with the supramolecular reagent isonicotinamide . Andreas Lemmerer, Manuel A. Fernandes
, New J. Chem.
, 2012
, 36
, 2242
Advances in the catalytic asymmetric synthesis of quaternary carbon containing cyclobutanes . Kai-Ge Wen, Yi-Yuan Peng, Xing-Ping Zeng
, Org. Chem. Front.
, 2020
, 7
, 2576
Catalytic asymmetric synthesis of α-stereogenic carboxylic acids: recent advances . Rui Niu, Yi He, Jun-Bing Lin
, Org. Biomol. Chem.
, 2022
, 20
, 37
Infrared spectral charateristics of the cyclobutane ring system . Karimullah A. Zirvi, Charles H. Jarboe
, J. Chem. Soc. B
, 1971
, 1603
Merging C(sp3 )–H activation with DNA-encoding . Zhoulong Fan, Shuai Zhao, Tao Liu, Peng-Xiang Shen, Zi-Ning Cui, Zhe Zhuang, Qian Shao, Jason S. Chen, Anokha S. Ratnayake, Mark E. Flanagan, Dominik K. Kölmel, David W. Piotrowski, Paul Richardson, Jin-Quan Yu
, Chem. Sci.
, 2020
, 11
, 12282
Incorporation of a cyclobutyl substituent in molecules by transition metal-catalyzed cross-coupling reactions . Janine Cossy, Peter Polàk, Paul C. Ruer
, Org. Biomol. Chem.
, 2022
, 20
, 7529
Structure-affinity relationships of reversible proline analog inhibitors targeting proline dehydrogenase . Alexandra N. Bogner, John J. Tanner
, Org. Biomol. Chem.
, 2022
, 20
, 895
Spectroscopic studies. Part IX. Infrared spectra and structure of some cyclobutanecarboxylic acids . T. H. Thomas, A. J. S. Williams, W. J. Orville-Thomas
, J. Chem. Soc. B
, 1968
, 908
Diastereoselective palladium-catalyzed functionalization of prochiral C(sp3 )–H bonds of aliphatic and alicyclic compounds . Srinivasarao Arulananda Babu, Yashika Aggarwal, Pooja Patel, Radha Tomar
, Chem. Commun.
, 2022
, 58
, 2612