Reactions of Alkynyldihaloboranes with 1,3-Dienes. 1,4-Alkynylborations and Stepwise Diels−Alder Reactions
Author:
Affiliation:
1. Department of Chemistry, Texas A&M University, College Station, Texas 77843-3255
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo961892h
Reference19 articles.
1. High reactivity, regioselectivity, and endo-stereoselectivity of vinyl boranes in Diels-Alder reactions
2. Tuning of Vinylborane Dienophilicity. Optimization of Reactivity, Regioselectivity, endo-Stereoselectivity, and Reagent Stability
3. An unprecedented electronic preference for the "meta" product in Diels-Alder reactions of ethynyldialkylboranes. [(Trimethylsilyl)ethynyl]-9-BBN as a reactive and versatile dienophile
4. A [4 + 3] transition state for a [4 + 2] cycloaddition. A new secondary orbital interaction in Diels-Alder reactions
5. In situ formation of vinylboranes for use in Diels Alder reactions. An easy one-pot Diels-Alder synthesis of cyclohexenols
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1. Unsaturated (C(sp2/sp)–B) Boronic Acid Derivatives;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2024
2. Detours in the Development of the Organocatalytic Diels‐Alder Reactions of Vinylboronic Compounds. A Dead End?;European Journal of Organic Chemistry;2023-01-30
3. Synthesis and reactivity of alkynyl boron compounds;Organic & Biomolecular Chemistry;2021
4. Stereoselective [4+2]‐Cycloaddition with Chiral Alkenylboranes;Angewandte Chemie International Edition;2020-05-11
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