( R )1‐(+)1‐Pantolactone Acrylate as a Chiral Auxiliary in the Baylis‐Hillman Reaction
Author:
Affiliation:
1. Department of Chemistry, University of Natal, Pietermaritzburg 3200, Republic of South Africa
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19931260631
Reference20 articles.
1. Facile Diastereoselective Synthesis of 2,6‐Dialkyl‐5‐methylene‐1,3‐dioxan‐4‐ones via α‐Activated Vinyl Esters
2. Synthetic potential of the tertiary-amine-catalysed reaction of activated vinyl carbanions with aldehydes
3. Optisch aktive Alkohole aus 1,3-Dioxan-4-onen; eine praktikable Variante der asymmetrischen Synthese unter nucleophiler Substitution an Acetalzentren
4. Preparation of Optically Active Alcohols from 1,3-Dioxan-4-ones. A Practical Version of the Asymmetric Synthesis with Nucleophilic Substitution at Acetal Centers
5. J. H.Hennes D. G.Grundiger U.S. Patent 2854460 1958;
Cited by 26 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Mechanistic Options for the Morita-Baylis-Hillman Reaction (n?→?π*);Lewis Base Catalysis in Organic Synthesis;2016-08-17
2. The Morita-Baylis-Hillman Reaction: Advances and Contributions from Brazilian Chemistry;Current Organic Synthesis;2015-08-28
3. Protection for the Carbonyl Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
4. A Bifunctional β-Isocupreidine Derivative as Catalyst for the Enantioselective Morita-Baylis-Hillman Reaction and a Mechanistic Rationale for Enantioselectivity;European Journal of Organic Chemistry;2012-06-15
5. Morita–Baylis–Hillman Reaction;The Chemistry of the Morita-Baylis-Hillman Reaction;2011-04-04
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3