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Shahien Shahsavari

SchoolVc-academic Affairs
Address9500 Gilman Drive #
La Jolla CA 92093
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    1. Oligodeoxynucleotide Synthesis Under Non-Nucleophilic Deprotection Conditions. Curr Protoc. 2024 Feb; 4(2):e983. Fang S, Chillar K, Yin Y, Apostle A, Eriyagama DNAM, Shahsavari S, Halami B, Yuan Y. PMID: 38327123; PMCID: PMC10857739.
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    2. Oligonucleotide synthesis under mild deprotection conditions. New J Chem. 2023 May 14; 47(18):8714-8722. Chillar K, Eriyagama AMDN, Yin Y, Shahsavari S, Halami B, Apostle A, Fang S. PMID: 37915883; PMCID: PMC10617641.
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    3. Dim and Dmoc Protecting Groups for Oligodeoxynucleotide Synthesis. Curr Protoc Nucleic Acid Chem. 2020 09; 82(1):e111. Fang S, Eriyagama D, Yuan Y, Shahsavari S, Chen J, Lin X, Halami B. PMID: 32628352; PMCID: PMC7449763.
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    4. Sensitive Oligodeoxynucleotide Synthesis Using Dim and Dmoc as Protecting Groups. J Org Chem. 2019 11 01; 84(21):13374-13383. Shahsavari S, Eriyagama DNAM, Chen J, Halami B, Yin Y, Chillar K, Fang S. PMID: 31536351; PMCID: PMC6825528.
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    5. Electrophilic oligodeoxynucleotide synthesis using dM-Dmoc for amino protection. Beilstein J Org Chem. 2019; 15:1116-1128. Shahsavari S, Eriyagama DNAM, Halami B, Begoyan V, Tanasova M, Chen J, Fang S. PMID: 31164948; PMCID: PMC6541367.
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    6. Parallel, Large-Scale, and Long Synthetic Oligodeoxynucleotide Purification Using the Catching Full-Length Sequence by Polymerization Technique. Org Process Res Dev. 2018 Sep 21; 22(9):1282-1288. Eriyagama DNAM, Shahsavari S, Halami B, Lu BY, Wei F, Fang S. PMID: 30906183; PMCID: PMC6428204.
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    7. Incorporation of Sensitive Ester and Chloropurine Groups into Oligodeoxynucleotides through Solid Phase Synthesis. ChemistrySelect. 2018 Aug 23; 3(31):8857-8862. Halami B, Shahsavari S, Nelson Z, Prehoda L, Eriyagama DNAM, Fang S. PMID: 30886889; PMCID: PMC6420219.
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    8. An amine protecting group deprotectable under nearly neutral oxidative conditions. Beilstein J Org Chem. 2018; 14:1750-1757. Shahsavari S, McNamara C, Sylvester M, Bromley E, Joslin S, Lu BY, Fang S. PMID: 30112080; PMCID: PMC6071699.
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    9. dM-Dim for Carboxylic Acid Protection. Tetrahedron Lett. 2018 May 02; 59(18):1763-1766. Shahsavari S, Wigstrom T, Gooding J, McNamara C, Fang S. PMID: 30275612; PMCID: PMC6161831.
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    10. Formation of Hindered Arylcarbamates using Alkyl Aryl Carbonates under Highly Reactive Conditions. ChemistrySelect. 2017 May 02; 2(13):3959-3963. Shahsavari S, Gooding J, Wigstrom T, Fang S. PMID: 29098174; PMCID: PMC5662102.
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    11. Synthesis of Oligodeoxynucleotides Containing Electrophilic Groups. Org Lett. 2016 08 05; 18(15):3870-3. Lin X, Chen J, Shahsavari S, Green N, Goyal D, Fang S. PMID: 27447361; PMCID: PMC4975647.
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    12. Tritylation of Alcohols under Mild Conditions without Using Silver Salts. Tetrahedron Lett. 2016 Aug 24; 57(34):3877-3880. Shahsavari S, Chen J, Wigstrom T, Gooding J, Gauronskas A, Fang S. PMID: 28042179; PMCID: PMC5193390.
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