[2:1] and [2:2] cycloadducts from N-sulfonylamines and azomethines

2:1] and [2:2] Cycloadducts from N-Sulfonylamines and Azomethines. -The cycloaddition of N-sulfonylamine (I) with azomethine (II) gives 2:1 cycloadduct (III). 3,4-Dihydroisoquinoline (V) reacts under similar conditions via a highly unusual cycloaddition pathway furnishing the 2:2 cycloadduct (VI). -(LENDER, A.; WALKER, N. P. C.; SCHAUMANN*, E.; Tetrahedron Lett. 56 (2015) 33, 4800-4803, http://dx.

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ChemInform Abstract: [2:1] and [2:2] Cycloadducts from N‐Sulfonylamines and Azomethines.

Lender

Walker

Schaumann

2015

ChemInform

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Synthesis of new class of trithiadiazacycloalkane 1,1-dioxides using Yb(Sm)-contaning catalysts and conformational analysis of the macroheterocycles

Khairullina,

Tyumkina

2024

Chem Heterocycl Comp

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Generation and precise control of sulfonyl radicals: visible-light-activated redox-neutral formation of sulfonates and sulfonamides

Zhang

Ding

et al. 2021

Org. Chem. Front.

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[2:1] and [2:2] cycloadducts from N-sulfonylamines and azomethines

Cited by 5 publications

References 21 publications

ChemInform Abstract: [2:1] and [2:2] Cycloadducts from N‐Sulfonylamines and Azomethines.

ChemInform Abstract: [2:1] and [2:2] Cycloadducts from N‐Sulfonylamines and Azomethines.

Synthesis of new class of trithiadiazacycloalkane 1,1-dioxides using Yb(Sm)-contaning catalysts and conformational analysis of the macroheterocycles

Generation and precise control of sulfonyl radicals: visible-light-activated redox-neutral formation of sulfonates and sulfonamides

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