Explore tweets tagged as #Macrocyclization
Catalytic Enantioselective Synthesis of Planar-Chiral Cyclophanes via a Chiral Octahedral Cobalt(III)-Templated C–H Macrocyclization https://t.co/U8lcr7Qwk2
@J_A_C_S @isciverse #Chemistry #chemed #scicomm #news #Technology #Tech #TIC2025 #research #science #AcademicTwitter
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.@CCSChemistry Article Highlight: Organocatalytic intramolecular enantioselective, atropselective, and diastereoselective macrocyclization of quinone methylidenes with alcohols Click to read: https://t.co/I78t3LqSUW
#chemistry #openaccess #science #chemtwitter
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#TotalSynthesis of (−)-Enigmazole A by the Macrocyclization/Transannular Pyran Cyclization Strategy: Application to Structure–Activity Relationship Investigations by Kyoya Ohyama, Taisei Masuda, Keita Sakamoto, Atsushi Yoshimura, Kyoko Tatsumoto, Keisuke Murata, and Haruhiko
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Enantioselective macrocyclization via catalytic metallic dipole relay https://t.co/biLCY53YRk
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Catalytic Enantioselective Synthesis of Planar-Chiral Cyclophanes via a Chiral Octahedral Cobalt(III)-Templated C–H Macrocyclization | Journal of the American Chemical Society
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Dec issue live🎉 Generating antiaromaticity N-alkyl aniline synthesis Electrochemical amination CO to CH3OH Allylic fluoroalkylation of terpenes TM-free C(sp2)–C(sp3) cross-coupling Enantiocontrolled macrocyclization C(sp3)–H alkylation polymerization https://t.co/iArfuT0Usc
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Enantioselective macrocyclization via catalytic metallic dipole relay https://t.co/iopAUuWf5K
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Highly Distorted Porous Nanographenes: Saddle-shaped nanographenes with a fenestrindane core synthesized by a fourfold intramolecular Yamamoto macrocyclization https://t.co/UALSvPPCNk
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Online now: Chemically revertible molecular clasps: Hydroxamic acid-mediated peptide macrocyclization and linearization https://t.co/NFdHY1dY3p
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Chemoselective Sulfonyl Fluoride Exchange (SuFEx)-Induced Macrocyclization of Tyrosine-Containing Peptides in Aqueous Media
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#BiomimeticSynthesis of Chejuenolides A−C by a Cryptic LactoneBased Macrocyclization: Stereochemical Implications in #Biosynthesis by Bingbing Zhang, Kuan Zheng, and Ran Hong at the Shanghai Institute of Organic Chemistry in @ACSCentSci
https://t.co/Wfy3XvDhC8
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One-Step Catalyst-Transfer Macrocyclization: Expanding the Chemical Space of Azaparacyclophanes @J_A_C_S #Chemistry #Chemed #Science #TechnologyNews #news #technology #AcademicTwitter #ResearchPapers
https://t.co/eWxyJ9hOQt
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We presented posters about FKBP12 based molecular glues targeting BRD4 and the potential of Macrocyclization to improve aqueous solubility at the FiMC conference in Munich.
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Second, the peptide-EBXs from Xingyu @Xingyuu_Liu (previously on @ChemRxiv ) also accepted @angew_chem ! A huge work @ERC_Research including thiol functionalization, photocatalyzed macrocyclization and binding studies with Heinis group @EPFL_CHEM_Tweet
https://t.co/EYKEYx5Q1a
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Remarkably facile ring-size control in macrocyclization: synthesis of hemicucurbit[6]uril and hemicucurbit[12]uril https://t.co/iKiOvIbTAH
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Self‐Contained Calix[3]Acridans with Macrocyclization Induced TADF Property for Highly Selective Recognition of Fe3+ and Detection of Oxidation Degree of Pyrite Medicinal Herbs
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Hybrid materials comprising ferrocene and diaminoborane moieties: linear concatenation versus macrocyclization (@ChemCommun): https://t.co/YLoQaqLtG5 (@HeltenGroupJMU).
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How easy is on-resin peptide macrocyclization? Find a rapid, efficient, and operationally simple disulfide-driven peptide macrocyclization method for synthesizing peptide drugs on a solid phase in this #OrgLett article from Bandyopadhyay & team @AB_IITRPR
https://t.co/X0QFBRGxQF
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On the cover of this week's issue [ https://t.co/BpC2J1dgRj] of #OrgLett: DABCO-based cations, forming exceptionally stable complexes with prism[5]arenes, significantly boost macrocyclization yields, streamline purification, and reduce waste. [ https://t.co/2YenGvKQop]
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The GCI was delighted to host Professor Shawn Collins for an incredible talk on catalysis, macrocyclization, and green chemistry @chemuoft @chimie_UdeM We are looking forward to even more future knowledge sharing and collaborative efforts!
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