Synthesis with silicon templates: preparation of macrocyclic amides

Schwartz, E. M.; Shanzer, Abraham

doi:10.1039/c39810000634

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It Was Thenthoughtthat Replacing the Oxygen Heteroatom By Ni1

Macrocyclic Compounds With Mirror Symmetry1

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1983

2005

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Cited by 12 publications

(2 citation statements)

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“…The synthesis of the macrocyclic amides was achieved by the use of cyclic silicon-nitrogen compounds (21). In these reactions both macrocyclic diamides and tetramides were obtained, depending on the nature of the constituents.…”

Section: It Was Thenthoughtthat Replacing the Oxygen Heteroatom By Nimentioning

confidence: 99%

Large Ring Heterocycles: Template Synthesis and Structure

Shanzer

1983

Bulletin des Soc Chimique

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Section: It Was Thenthoughtthat Replacing the Oxygen Heteroatom By Nimentioning

confidence: 99%

Large Ring Heterocycles: Template Synthesis and Structure

Shanzer

1983

Bulletin des Soc Chimique

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“…Macrocyclic diamides 9a or tetramides 9 were obtained, depending on the nature of the diamine and diacyl reactants. 20 Diamines with even-numbered methylene chains formed macrocyclic diamides with even diacyl dihalides and macrocyclic tetramides 9 with odd diacyl dihalides. On the other (29) M. Mortality and J. M. Kliegman, J. Org.…”

Section: Macrocyclic Compounds With Mirror Symmetrymentioning

confidence: 99%