Skeletal Alkylcarbonation (SAC) Reactions as a Simple Design for Cluster-Carbon Insertion and Cross-Coupling: High-Yield Access to Substituted Tricarbollides from 6,9-Dicarba-arachno-decaborane(14)
Author:
Publisher
Wiley
Subject
General Chemistry,Catalysis,Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201102016/fullpdf
Reference18 articles.
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3. Monocarbaborane Anion Chemistry. Syntheses and Structures Within the closo Nine-Vertex System
4. New carboranes and phosphaboranes
5. Synthesis, molecular structure, and nuclear magnetic resonance spectra of the anionic monocarbametallaborane [NEt4][(CO)3(PPh3)(OH)-closo-MoCB10H10]·CH2Cl2
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1. Open-face alkylation of the 8-R-nido-7,8,9-C3B8H11 tricarbollides;Journal of Organometallic Chemistry;2016-11
2. An unexpected rearrangement of carbon vertexes in the tricarbollide series. Asymmetrical 7-aryl-nido-7,8,9-C3B8H11 derivatives;Journal of Organometallic Chemistry;2016-03
3. Eleven-Vertex Carboranes;Carboranes;2016
4. Unique Stereocontrol in Carborane Chemistry: Skeletal Alkylcarbonation (SAC) versus Exoskeletal Alkylmethylation (EAM) Reactions;Angewandte Chemie International Edition;2015-02-23
5. Unique Stereocontrol in Carborane Chemistry: Skeletal Alkylcarbonation (SAC) versus Exoskeletal Alkylmethylation (EAM) Reactions;Angewandte Chemie;2015-02-23
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