Novel Coupling Reactions of Dithioacetals with Organocuprate Reagents. Propargylic Dithioacetal as an Allene - 1,3-Zwitterion Synthon

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Tseng, H.-R.

Luh, T.-Y.

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Journal of Organic Chemistry | / 62卷 / 14期

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[1] Novel coupling reactions of dithioacetals with organocuprate reagents. Propargylic dithioacetal as an allene-1,3-zwitterion synthon
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JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (14): : 4568 - 4569
[2] Propargylic dithioacetal as an allene 1,3-dication synthon. Nickel-catalyzed cross-coupling reactions of propargylic dithioacetals with grignard reagents
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[3] Dithioacetal as a 1,1-zwitterion synthon. Synthesis of functionalized alkenes by the coupling of benzylic dithioacetals with another 1,1-zwitterion synthon
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[4] Allylic dithioacetal as a propene-1,3-zwitterion synthon. Regioselective conversion of C-S bonds in allylic dithioacetals into C-C bonds
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[5] Dithioacetal as a 1,1-zwitterion synthon. Synthesis of functionalized alkenes by the coupling of benzylic dithioacetals with another 1,1-zwitterion synthon (vol 46, pg 771, 2005)
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TETRAHEDRON LETTERS, 2005, 46 (10) : 1765 - 1765
[6] TRANSITION-METAL PROMOTED REACTIONS .30. CYCLOPROPYL ANION AS AN ALLYL ANION SYNTHON - NOVEL SYNTHESIS OF BUTADIENES BY NICKEL-CATALYZED COUPLING OF CYCLOPROPYL GRIGNARD-REAGENTS WITH DITHIOACETALS
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