Reactions · Organic Syntheses ↗
Synthesis of Arylboronic Pinacol Esters from Corresponding Arylamines
Rearrangement
Overview
Preparation of Synthesis of Arylboronic Pinacol Esters from Corresponding Arylamines. Submitted by Di Qiu, He Meng, Liang Jin, Shengbo Tang, Shuai Wang, Fangyang Mo, Yan Zhang and Jianbo Wang*1. DOI: 10.15227/orgsyn.091.0106.
Actions
- This entry doesn't have stoichiometric equivalents on file yet — the Reaction Scale Calculator needs at least one participant tagged with an equivalents value.
- Mechanism / source ↗
- View as JSON ↗
Search literature
More Rearrangement reactions
- 1,2-METALLATE REARRANGEMENT: (Z)-4-(2-PROPENYL)-3-OCTEN-1-OL (3-Octen-1-ol, 4-(2-propenyl)-, (Z)-) Rearrangement
- 1-N-ACYLAMINO-1,3-DIENES FROM 2,4-PENTADIENOIC ACIDS BY THE CURTIUS REARRANGEMENT: BENZYL trans-1,3-BUTADIENE-1-CARBAMATE (Carbamic acid, 1,3-butadienyl-, (E)-, phenylmethyl ester) Rearrangement
- ALKENES via HOFMANN ELIMINATION: USE OF ION-EXCHANGE RESIN FOR PREPARATION OF QUATERNARY AMMONIUM HYDROXIDES: DIPHENYLMETHYL VINYL ETHER (Benzene, 1,1'-[(ethenyloxy)methylene]bis-) Rearrangement
- Allen–Millar–Trippett rearrangement Rearrangement
- Allyl Cyanate-To-Isocyanate Rearrangement: Preparation of tert-Butyl 3,7-dimethylocta-1,6-dien-3-ylcarbamate Rearrangement
- Amadori rearrangement Rearrangement