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- Reactivity of thionitrate esters: putative intermediates in nitrovasodilator activity. Jennifer D. Artz, Kexin Yang, Jodi Lock, Cristina Sanchez, Brian M. Bennett, Gregory R. J. Thatcher
, Chem. Commun.
, 1996
, 927
- Synthesis and characterization of enantiopure chiral NH2/SO palladium complexes. Nazaret Moreno-Rodriguez, L. Gabriel Borrego, Rocío Recio, Victoria Valdivia, M. Carmen Nicasio, Eleuterio Álvarez, Noureddine Khiar, Inmaculada Fernández
, Org. Biomol. Chem.
, 2023
, 21
, 5827
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Chelation-assisted nucleophilic aromatic substitution of
2-sulfonyl-substituted 1-methoxynaphthalenes by Grignard reagents:
factors determining the activating ability of the 2-sulfonyl
substituents 1,2
. Tetsutaro Hattori, Mikio Suzuki, Noriyuki Tomita, Ayanobu Takeda, Sotaro Miyano
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 1117
- Nickel-catalysed substitutions of aryl tert-butyl sulfones with organometallic reagents: synthesis of ortho-substituted unsymmetrical biaryls. Jonathan Clayden, J. Jonathan A. Cooney, Marc Julia
, J. Chem. Soc., Perkin Trans. 1
, 1995
, 7
- ortho-Substituted unsymmetrical biaryls from aryl tert-butyl sulfones. Jonathan Clayden, Marc Julia
, J. Chem. Soc., Chem. Commun.
, 1993
, 1682
- Synthetic studies related to the esperamicin/calicheamicin aglycone: efficient construction of a homochiral oxabicyclo [7 : 3 : 1] analogue from D-xylose. Isabelle Dancy, Troels Skrydstrup, Christophe Crévisy, Jean-Marie Beau
, J. Chem. Soc., Chem. Commun.
, 1995
, 799
- A truce on the Smiles rearrangement: revisiting an old reaction—the Truce–Smiles rearrangement. Timothy J. Snape
, Chem. Soc. Rev.
, 2008
, 37
, 2452
- Allylic sulfones as allyl anion equivalents: homoallylic alcohols from metal catalysed reactions of sulfones with aldehydes and ketones. Jonathan Clayden, Marc Julia
, J. Chem. Soc., Chem. Commun.
, 1994
, 1905
- Homoallylic alcohols from samarium diiodide-mediated coupling of allylic sulfones with carbonyl compounds. Jonathan Clayden, Marc Julia
, J. Chem. Soc., Chem. Commun.
, 1994
, 2261