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Beilstein J. Org. Chem. 2011, 7, 9–12, doi:10.3762/bjoc.7.2
Graphical Abstract
Figure 1: tert-Butylsulfinamide.
Scheme 1: Synthesis of acid amide.
Figure 2: N-(tert-butylthio)-tert-butylsulfonamide.
Scheme 2: Chemical synthesis of 3.
Figure 3: ORTEP diagram of 3.
Scheme 3: Synthesis of tert-butylsulfanyl chloride.
Scheme 4: Synthesis of tert-butylsulfonamide.
Scheme 5: Proposed mechanism for rearrangement.
Beilstein J. Org. Chem. 2007, 3, No. 20, doi:10.1186/1860-5397-3-20
Scheme 1: Conversion of coumarin-4-one oximes to 3-alkyl-1,2-benzisoxazole derivatives.
Scheme 2: Reactions of 3-halomethyl derivatives with other nucleophiles.
Scheme 3: Sultone oximes and its precursor ketones.
Scheme 4: Synthesis of 1,2-benzoxathiin-4(3H)-one-2,2-dioxide 6 from methanesulfonate of salicylaldehyde.
Scheme 5: Preparation of 1,2-benzoxathiin-4(3H)-one-2,2-dioxides.
Scheme 6: Preparation of sultone oximes.
Scheme 7: Preparation of 3-alkyl-1,2-benzisoxazole derivatives.
Scheme 8: Synthesis of zonisamide from 1,2-benzisoxazole-3-methane-sulfonate.