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Ring opening polymerization of oxetane by the use of a montmorillonite clay  as catalyst - ScienceDirect
Ring opening polymerization of oxetane by the use of a montmorillonite clay as catalyst - ScienceDirect

Oxetanes - an overview | ScienceDirect Topics
Oxetanes - an overview | ScienceDirect Topics

Anionic polymerization of activated oxetane and its copolymerization with  ethylene oxide for the synthesis of amphiphilic block copolymers - Polymer  Chemistry (RSC Publishing) DOI:10.1039/C8PY00307F
Anionic polymerization of activated oxetane and its copolymerization with ethylene oxide for the synthesis of amphiphilic block copolymers - Polymer Chemistry (RSC Publishing) DOI:10.1039/C8PY00307F

AM mechanism for polymerization of oxetane ring. | Download Scientific  Diagram
AM mechanism for polymerization of oxetane ring. | Download Scientific Diagram

Radical Ring-Opening of Oxetanes Enabled by Co-Catalysis | Organic  Chemistry | ChemRxiv | Cambridge Open Engage
Radical Ring-Opening of Oxetanes Enabled by Co-Catalysis | Organic Chemistry | ChemRxiv | Cambridge Open Engage

Cationic ring opening polymerization of oxetane proceeds through the... |  Download Scientific Diagram
Cationic ring opening polymerization of oxetane proceeds through the... | Download Scientific Diagram

Radical Ring-Opening of Oxetanes Enabled by Co-Catalysis | Organic  Chemistry | ChemRxiv | Cambridge Open Engage
Radical Ring-Opening of Oxetanes Enabled by Co-Catalysis | Organic Chemistry | ChemRxiv | Cambridge Open Engage

PDF] Enantioselective Oxetane Ring Opening with Chloride: Unusual Use of  Wet Molecular Sieves for the Controlled Release of HCl. | Semantic Scholar
PDF] Enantioselective Oxetane Ring Opening with Chloride: Unusual Use of Wet Molecular Sieves for the Controlled Release of HCl. | Semantic Scholar

Regioselective ring opening reactions of unsymmetric oxetanes | Download  Scientific Diagram
Regioselective ring opening reactions of unsymmetric oxetanes | Download Scientific Diagram

Catalytic asymmetric nucleophilic openings of 3-substituted oxetanes -  Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C4OB00920G
Catalytic asymmetric nucleophilic openings of 3-substituted oxetanes - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C4OB00920G

Mild C–C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with  Soft Carbon Nucleophiles - Huang - 2021 - Angewandte Chemie International  Edition - Wiley Online Library
Mild C–C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with Soft Carbon Nucleophiles - Huang - 2021 - Angewandte Chemie International Edition - Wiley Online Library

Mild C–C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with  Soft Carbon Nucleophiles - Huang - 2021 - Angewandte Chemie International  Edition - Wiley Online Library
Mild C–C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with Soft Carbon Nucleophiles - Huang - 2021 - Angewandte Chemie International Edition - Wiley Online Library

2-Debenzoyl Paclitaxel , Oxetane ring-opened, 2, 20-oxolane - Phyton Biotech
2-Debenzoyl Paclitaxel , Oxetane ring-opened, 2, 20-oxolane - Phyton Biotech

Ring-opening reactions of oxetanes: A review of methodology development and  synthetic applications
Ring-opening reactions of oxetanes: A review of methodology development and synthetic applications

IJMS | Free Full-Text | Chemical Space Exploration of Oxetanes
IJMS | Free Full-Text | Chemical Space Exploration of Oxetanes

Enantioselective Oxetane Ring Opening with Chloride: Unusual Use of Wet  Molecular Sieves for the Controlled Release of HCl - Yang - 2016 -  Angewandte Chemie - Wiley Online Library
Enantioselective Oxetane Ring Opening with Chloride: Unusual Use of Wet Molecular Sieves for the Controlled Release of HCl - Yang - 2016 - Angewandte Chemie - Wiley Online Library

A mild catalytic synthesis of 2-oxazolines via oxetane ring-opening: rapid  access to a diverse family of natural products - Chemical Science (RSC  Publishing)
A mild catalytic synthesis of 2-oxazolines via oxetane ring-opening: rapid access to a diverse family of natural products - Chemical Science (RSC Publishing)

IJMS | Free Full-Text | Chemical Space Exploration of Oxetanes
IJMS | Free Full-Text | Chemical Space Exploration of Oxetanes

The I-V characteristics of organic hole-only devices based on crosslinked  hole-transport layer | Journal of Applied Research and Technology. JART
The I-V characteristics of organic hole-only devices based on crosslinked hole-transport layer | Journal of Applied Research and Technology. JART

Oxetane Substrates of Human Microsomal Epoxide Hydrolase | Drug Metabolism  & Disposition
Oxetane Substrates of Human Microsomal Epoxide Hydrolase | Drug Metabolism & Disposition

Scheme 9. Ring opening of oxetanes 18 under nonacidic conditions. |  Download Scientific Diagram
Scheme 9. Ring opening of oxetanes 18 under nonacidic conditions. | Download Scientific Diagram

Ring Expansions of Oxetanes
Ring Expansions of Oxetanes

Cationic ring opening polymerization of oxetane proceeds through the... |  Download Scientific Diagram
Cationic ring opening polymerization of oxetane proceeds through the... | Download Scientific Diagram

Ring-opening reactions of oxetanes: A review of methodology development and  synthetic applications
Ring-opening reactions of oxetanes: A review of methodology development and synthetic applications

Oxetanes - an overview | ScienceDirect Topics
Oxetanes - an overview | ScienceDirect Topics

Paclitaxel Oxetane Ring-Opened 3-Acetyl 4-Benzoyl Impurity- Paclitaxel  Impurities | CLEARSYNTH
Paclitaxel Oxetane Ring-Opened 3-Acetyl 4-Benzoyl Impurity- Paclitaxel Impurities | CLEARSYNTH