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Managing Systems Development Term Paper Leap integrated ticketing system
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NCH 2777
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1,1-Disilyl Alcohols as d1 Synthons: Harnessing the 1,2-Brook Rearrangement
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Orbital interaction theory of organic chemistry. Arvi Rauk. 2nd edn. John Wiley & Sons, Ltd, Chichester, 2001. xv + 343 pages. £67.50. ISBN 0-471-35833-9
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ChemInform Abstract: Silyl-cupration of an Acetylene Followed by Ring-Formation
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ChemInform Abstract: Decarboxylative Elimination of Enol Triflates as a General Synthesis of Acetylenes
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ChemInform Abstract: Unusual Cyclopropanol Formation from a β-Silyl Aldehyde
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ChemInform Abstract: Trapping the Tetrahedral Intermediate in the 1,3-Shift of an Acetyl Group Using a Triisopropylsilyl Group
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1,1-Disilyl Alcohols as d1 Synthons: Harnessing the 1,2-Brook Rearrangement
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β-Silyl Carbonyl Compounds
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Decarboxylative Elimination of Enol Triflates as a General Synthesis of Acetylenes
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The Phenyldimethylsilyllithium Reagent
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The total synthesis of (± )-trichostatin A : Some observations on the acylation and alkylation of silyl enol ethers, silyl dienol ethers and a silyl trienol ether
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The stereospecific synthesis of a carbacyclin analogue using the protodesilylation of an allylsilane
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Silyl-cupration of an acetylene followed by ring-formation
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A regiocontrolled synthesis of allylstannanes
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Two new stereochemically complementary oxindole synthesis
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