Search Results - Chaminda Lakmal, Hetti Handi

  • Showing 1 - 9 results of 9
Refine Results
  1. 1
    Ruthenium-Catalyzed Enantioselective C–H Functionalization: A Practical Access to Optically Active Indoline Derivatives

    Ruthenium-Catalyzed Enantioselective C–H Functionalization: A Practical Access to Optically Active Indoline Derivatives by Li, Zhong-Yuan, Lakmal, Hetti Handi Chaminda, Qian, Xiaolin, Zhu, Zhenyu, Donnadieu, Bruno, McClain, Sarah J, Xu, Xue, Cui, Xin

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Enabling Catalytic Arene C–H Amidomethylation via Bis(tosylamido)methane as a Sustainable Formaldimine Releaser

    Enabling Catalytic Arene C–H Amidomethylation via Bis(tosylamido)methane as a Sustainable Formaldimine Releaser by Li, Zhong-Yuan, Chaminda Lakmal, Hetti Handi, Cui, Xin

    Published in Organic letters
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    Fe(III)-Based Tandem Catalysis for Amidomethylative Multiple Substitution Reactions of α‑Substituted Styrene Derivatives

    Fe(III)-Based Tandem Catalysis for Amidomethylative Multiple Substitution Reactions of α‑Substituted Styrene Derivatives by Qian, Xiaolin, Zhou, Hui, Chaminda Lakmal, Hetti Handi, Lucore, James, Wang, Xuesong, Valle, Henry U, Donnadieu, Bruno, Xu, Xue, Cui, Xin

    Published in ACS catalysis
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  4. 4
    Improvement of the Metabolic Stability of GPR88 Agonist RTI-13951-33: Design, Synthesis, and Biological Evaluation

    Improvement of the Metabolic Stability of GPR88 Agonist RTI-13951-33: Design, Synthesis, and Biological Evaluation by Rahman, Md Toufiqur, Decker, Ann M., Ben Hamida, Sami, Perrey, David A., Chaminda Lakmal, Hetti Handi, Maitra, Rangan, Darcq, Emmanuel, Kieffer, Brigitte L., Jin, Chunyang

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  5. 5
    Design, Synthesis, and Structure–Activity Relationship Studies of Novel GPR88 Agonists (4-Substituted-phenyl)acetamides Based on the Reversed Amide Scaffold

    Design, Synthesis, and Structure–Activity Relationship Studies of Novel GPR88 Agonists (4-Substituted-phenyl)acetamides Based on the Reversed Amide Scaffold by Rahman, Md Toufiqur, Guan, Dongliang, Chaminda Lakmal, Hetti Handi, Decker, Ann M., Imler, Gregory H., Kerr, Andrew T., Harris, Danni L., Jin, Chunyang

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  6. 6
    Synthesis of C‑Unsubstituted 1,2-Diazetidines and Their Ring-Opening Reactions via Selective N–N Bond Cleavage

    Synthesis of C‑Unsubstituted 1,2-Diazetidines and Their Ring-Opening Reactions via Selective N–N Bond Cleavage by Chaminda Lakmal, Hetti Handi, Xu, Joanna Xiuzhu, Xu, Xue, Ahmed, Bassem, Fong, Christopher, Szalda, David J, Ramig, Keith, Sygula, Andrzej, Webster, Charles Edwin, Zhang, Dongmao, Cui, Xin

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  7. 7
    Catalytic [2 + 2 + 2] cycloaddition with indium(iii)-activated formaldimines: a practical and selective access to hexahydropyrimidines and 1,3-diamines from alkenes

    Catalytic [2 + 2 + 2] cycloaddition with indium(iii)-activated formaldimines: a practical and selective access to hexahydropyrimidines and 1,3-diamines from alkenes by Zhou, Hui, Chaminda Lakmal, Hetti Handi, Baine, Jonathan M, Valle, Henry U, Xu, Xue, Cui, Xin

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  8. 8
    Catalytic [2 + 2 + 2] cycloaddition with indium(iii)-activated formaldimines: a practical and selective access to hexahydropyrimidines and 1,3-diamines from alkenesElectronic supplementary information (ESI) available. CCDC 1538722 and 1554489. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7sc02576a

    Catalytic [2 + 2 + 2] cycloaddition with indium(iii)-activated formaldimines: a practical and selective access to hexahydropyrimidines and 1,3-diamines from alkenesElectronic suppl... by Zhou, Hui, Chaminda Lakmal, Hetti Handi, Baine, Jonathan M, Valle, Henry U, Xu, Xue, Cui, Xin

    Get full text
    Article
    Save to List
    Saved in:
  9. 9
    Catalytic [2 + 2 + 2] cycloaddition with indium(iii)-activated formaldimines: a practical and selective access to hexahydropyrimidines and 1,3-diamines from alkenes† †Electronic supplementary information (ESI) available. CCDC 1538722 and 1554489. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7sc02576a Click here for additional data file. Click here for additional data file

    Catalytic [2 + 2 + 2] cycloaddition with indium(iii)-activated formaldimines: a practical and selective access to hexahydropyrimidines and 1,3-diamines from alkenes† †Electronic su... by Zhou, Hui, Chaminda Lakmal, Hetti Handi, Baine, Jonathan M., Valle, Henry U., Xu, Xue, Cui, Xin

    Get full text
    Article
    Save to List
    Saved in:

Search Tools: