2001
DOI: 10.1002/1521-3773(20010119)40:2<411::aid-anie411>3.0.co;2-i
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Bowl-Shaped Tris(2,6-diphenylbenzyl)tin Hydride: A Unique Reducing Agent for Radical and Ionic Chemistry

Abstract: Unique selectivity, hitherto not observable in ordinary radical and ionic reactions, is achieved with the bowl‐shaped tris(2,6‐diphenylbenzyl)tin hydride (TDTH; see structure), which has been successfully utilized as a new reducing agent.

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Cited by 35 publications
(1 citation statement)
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“…In 2021, Lautens’ group reported the Pd-catalyzed cyclization reaction of aryl active reagents tethering alkyne compounds (Scheme a), followed by Lewis acid-catalyzed isomerization to prepare benzofuran derivatives. Although many similar cyclization strategies have been reported, studies of the one-pot preparation of benzofuran skeletons and the introduction of reactive functional groups are still relatively rare …”
Section: Introductionmentioning
confidence: 99%
“…In 2021, Lautens’ group reported the Pd-catalyzed cyclization reaction of aryl active reagents tethering alkyne compounds (Scheme a), followed by Lewis acid-catalyzed isomerization to prepare benzofuran derivatives. Although many similar cyclization strategies have been reported, studies of the one-pot preparation of benzofuran skeletons and the introduction of reactive functional groups are still relatively rare …”
Section: Introductionmentioning
confidence: 99%