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- X-Ray crystal structure and Diels–Alder reactivity of the 3,4-dimethyl-2H-phosphole dimer. Guillaume de Lauzon, Claude Charrier, Hubert Bonnard, François Mathey, Jean Fischer, André Mitschler
, J. Chem. Soc., Chem. Commun.
, 1982
, 1272
- P-chiral 1-phosphanorbornenes: from asymmetric phospha-Diels–Alder reactions towards ligand design and functionalisation. Tobias Möller, Peter Wonneberger, Menyhárt B. Sárosi, Peter Coburger, Evamarie Hey-Hawkins
, Dalton Trans.
, 2016
, 45
, 1904
- Hetero-Diels–Alder reactions of 2H-phospholes with allenes: synthesis and functionalization of 6-methylene-1-phosphanorbornenes. Keke Zhang, Qiaoyu Zhang, Donghui Wei, Rongqiang Tian, Zheng Duan
, Org. Chem. Front.
, 2021
, 8
, 3740
- Reactions of phosphines with acetylenes. Part XIV. Isomeric 1 : 2 adducts from triarylphosphines and dimethyl acetylenedicarboxylate. A cyclopentenylidenephosphorane. N. E. Waite, John C. Tebby, R. S. Ward, M. A. Shaw, Dudley H. Williams
, J. Chem. Soc. C
, 1971
, 1620
- A new reaction of 1-(2,4,6-trialkylphenyl)phospholes with heteroaromatic character; aromatic electrophilic substitution under the conditions of Friedel–Crafts acylation. György Keglevich, Tungalag Chuluunbaatar, Beáta Dajka, András Dobó, Áron Szöllősy, László Töke
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 2895
- Nonbenzenoid aromaticity of 1-phosphafulvenes: synthesis of phosphacymantrenes. Yanjie Liu, Rongqiang Tian, Zheng Duan, François Mathey
, Dalton Trans.
, 2021
, 50
, 476
- Oxo-phospholes from the alkoxyphosphonium ylides formed in the reaction of trialkyl phosphites or dialkyl phosphonites with dimethyl acetylenedicarboxylate. Julian C. Caesar, D. Vaughan Griffiths, John C. Tebby
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 175
- Reactions of phosphines with acetylenes. Part VII. Structure revision of a rearranged 1:2 adduct of triphenylphosphine and dimethyl acetylenedicarboxylate. A stable 2H-phosph(V)ole. N. E. Waite, J. C. Tebby, R. S. Ward, D. H. Williams
, J. Chem. Soc. C
, 1969
, 1100
- An aromatic–antiaromatic switch in P-heteroles. A small change in delocalisation makes a big reactivity difference. László Nyulászi, Oldamur Hollóczki, Christophe Lescop, Muriel Hissler, Régis Réau
, Org. Biomol. Chem.
, 2006
, 4
, 996
- Synthesis of P-stereogenic 1-phosphanorbornane-derived phosphine–phosphite ligands and application in asymmetric catalysis. Kyzgaldak Ramazanova, Soumyadeep Chakrabortty, Bernd H. Müller, Peter Lönnecke, Johannes G. de Vries, Evamarie Hey-Hawkins
, RSC Adv.
, 2023
, 13
, 34439