Preparation and Diels–Alder/cross coupling reactions of a 2-diethanolaminoboron-substituted 1,3-diene

A 2-diethanolamine boronyl substituted 1,3-diene has been synthesized in high yield and characterized spectroscopically as well as by X-ray crystallography. This diene has then subsequently been used in a number of fast, high yielding Diels–Alder/cross coupling reactions.

Bibliographic Details
Main Authors: Liqiong Wang, Cynthia S. Day, Marcus W. Wright, Mark E. Welker
Format: Article
Language:English
Published: Beilstein-Institut 2009-09-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.5.45
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author Liqiong Wang
Cynthia S. Day
Marcus W. Wright
Mark E. Welker
author_facet Liqiong Wang
Cynthia S. Day
Marcus W. Wright
Mark E. Welker
author_sort Liqiong Wang
collection DOAJ
description A 2-diethanolamine boronyl substituted 1,3-diene has been synthesized in high yield and characterized spectroscopically as well as by X-ray crystallography. This diene has then subsequently been used in a number of fast, high yielding Diels–Alder/cross coupling reactions.
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spelling doaj.art-32636985508f422c8f6036c6a2312d122022-12-21T23:25:51ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972009-09-01514510.3762/bjoc.5.451860-5397-5-45Preparation and Diels–Alder/cross coupling reactions of a 2-diethanolaminoboron-substituted 1,3-dieneLiqiong Wang0Cynthia S. Day1Marcus W. Wright2Mark E. Welker3Department of Chemistry, Wake Forest University, P.O. Box 7486, Winston-Salem, NC 27109 (USA)Department of Chemistry, Wake Forest University, P.O. Box 7486, Winston-Salem, NC 27109 (USA)Department of Chemistry, Wake Forest University, P.O. Box 7486, Winston-Salem, NC 27109 (USA)Department of Chemistry, Wake Forest University, P.O. Box 7486, Winston-Salem, NC 27109 (USA)A 2-diethanolamine boronyl substituted 1,3-diene has been synthesized in high yield and characterized spectroscopically as well as by X-ray crystallography. This diene has then subsequently been used in a number of fast, high yielding Diels–Alder/cross coupling reactions.https://doi.org/10.3762/bjoc.5.45cross couplingDiels–Alderorganoboron
spellingShingle Liqiong Wang
Cynthia S. Day
Marcus W. Wright
Mark E. Welker
Preparation and Diels–Alder/cross coupling reactions of a 2-diethanolaminoboron-substituted 1,3-diene
Beilstein Journal of Organic Chemistry
cross coupling
Diels–Alder
organoboron
title Preparation and Diels–Alder/cross coupling reactions of a 2-diethanolaminoboron-substituted 1,3-diene
title_full Preparation and Diels–Alder/cross coupling reactions of a 2-diethanolaminoboron-substituted 1,3-diene
title_fullStr Preparation and Diels–Alder/cross coupling reactions of a 2-diethanolaminoboron-substituted 1,3-diene
title_full_unstemmed Preparation and Diels–Alder/cross coupling reactions of a 2-diethanolaminoboron-substituted 1,3-diene
title_short Preparation and Diels–Alder/cross coupling reactions of a 2-diethanolaminoboron-substituted 1,3-diene
title_sort preparation and diels alder cross coupling reactions of a 2 diethanolaminoboron substituted 1 3 diene
topic cross coupling
Diels–Alder
organoboron
url https://doi.org/10.3762/bjoc.5.45
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AT cynthiasday preparationanddielsaldercrosscouplingreactionsofa2diethanolaminoboronsubstituted13diene
AT marcuswwright preparationanddielsaldercrosscouplingreactionsofa2diethanolaminoboronsubstituted13diene
AT markewelker preparationanddielsaldercrosscouplingreactionsofa2diethanolaminoboronsubstituted13diene