Search Results - "Xie, Qiuzhe"

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  1. 1
    Asymmetric Catalysis Route to anti,anti Stereotriads, Illustrated by Applications

    Asymmetric Catalysis Route to anti,anti Stereotriads, Illustrated by Applications by Parker, Kathlyn A, Xie, Qiuzhe

    Published in Organic letters (03-04-2008)
    “…A short sequence based on asymmetric catalysis, chirality transfer, and an optimized carbometallation protocol gave an anti,anti stereotriad building block in…”
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  2. 2
    A Relay Ring-Closing Metathesis Synthesis of Dihydrooxasilines, Precursors of (Z)-Iodo Olefins

    A Relay Ring-Closing Metathesis Synthesis of Dihydrooxasilines, Precursors of (Z)-Iodo Olefins by Xie, Qiuzhe, Denton, Richard W, Parker, Kathlyn A

    Published in Organic letters (04-12-2008)
    “…A convenient Grubbs II metathesis provides dihydrooxasilines by relay RCM (RRCM). Dihydrooxasilines undergo ring opening to give Z-vinyl silanes. These can…”
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  3. 3
    Process Development and Synthesis of Birinapant: Large Scale Preparation and Acid-Mediated Dimerization of the Key Indole Intermediate

    Process Development and Synthesis of Birinapant: Large Scale Preparation and Acid-Mediated Dimerization of the Key Indole Intermediate by Deng, Yijun, Xie, Qiuzhe, LaPorte, Matthew G, Chasnoff, Anna T. A, Mortensen, Mark A, Patra, Debasis, Putrelo, Seth A, Antonovich, Robert S, Cao, Hong, Yan, Jun, Cooper, Arthur J, Rippin, Susan R, Alexander, Matthew D, Kumar, Pavan Tirunahari, Hendi, Mukta S, Lee, Yu-Hua, Haimowitz, Thomas, Condon, Stephen M

    Published in Organic process research & development (19-02-2016)
    “…Birinapant/TL32711 (1) is a novel bivalent antagonist of the inhibitor of apoptosis (IAP) family of proteins which is currently in clinical development for the…”
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  4. 4
    Part I. One-pot synthesis of secondary alcohols and one-pot asymmetric synthesis of secondary propargylic alcohols. Part II. Redox isomerization of secondary propargylic alcohols to enones. Part III. Synthesis study towards C9-C14 fragment of (+)-discodermolide. Part IV. Asymmetric synthesis of anti, anti-stereotriad building blocks for polypropionate natural products

    Part I. One-pot synthesis of secondary alcohols and one-pot asymmetric synthesis of secondary propargylic alcohols. Part II. Redox isomerization of secondary propargylic alcohols to enones. Part III. Synthesis study towards C9-C14 fragment of (+)-discodermolide. Part IV. Asymmetric synthesis of anti, anti-stereotriad building blocks for polypropionate natural products by Xie, Qiuzhe

    Published 01-01-2007
    “…Part I. Chiral secondary propargyl alcohols are versatile building blocks for fine chemicals, pharmaceuticals, and natural products. A convenient method for…”
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  5. 5
    Part I. One-pot synthesis of secondary alcohols and one-pot asymmetric synthesis of secondary propargylic alcohols. Part II. Redox isomerization of secondary propargylic alcohols to enones. Part III. Synthesis study towards C9-C14 fragment of (+)-discodermolide. Part IV. Asymmetric synthesis of anti, anti-stereotriad building blocks for polypropionate natural products

    Part I. One-pot synthesis of secondary alcohols and one-pot asymmetric synthesis of secondary propargylic alcohols. Part II. Redox isomerization of secondary propargylic alcohols to enones. Part III. Synthesis study towards C9-C14 fragment of (+)-discodermolide. Part IV. Asymmetric synthesis of anti, anti-stereotriad building blocks for polypropionate natural products by Xie, Qiuzhe

    “…Part I. Chiral secondary propargyl alcohols are versatile building blocks for fine chemicals, pharmaceuticals, and natural products. A convenient method for…”
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    Dissertation
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