Pyramidalized olefins: The stereospecific conjugate reduction of a bicyclo[2.2.2]octadiene
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Origin of Huisgen's factor x: staggering of allylic bonds promotes anomalously rapid exo attack on norbornenes
2. The Reaction of Difluorocarbene with Bicyclo[2.2.2]octadiene
3. Stereoselectivities of dichloroketene cycloadditions to bridged bicyclic olefins
4. Unusual stereoselectivity in the Diels-Alder addition of cyclopentadiene with the bicyclo[2.2.2]octene nucleus
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1. Geometrical Dependence of the Highest Occupied Molecular Orbital in Bicyclic Systems: π-Facial Stereoselectivity of Bicyclic and Tricyclic Olefins;Asian Journal of Organic Chemistry;2015-05-29
2. Cycloadditions and Cyclizations of Acetylenic, Allenic, and Conjugated Dienyl Sulfones;Chemical Reviews;2010-05-04
3. A Theoretical Study of Tricyclo[4.2.1.02,5]non-2(5)-ene, Tricyclo[4.2.2.02,5]dec-2(5)-ene and Related Pyramidalized Alkenes;European Journal of Organic Chemistry;2007-09
4. Synthesis and Structure of Cyclopropano-Annelated Homosesquinorbornene Derivatives Containing Pyramidalized Double Bonds: Evidence for the Sterical Effect of a Cyclopropyl Group on the Degree of CC Double-Bond Pyramidalization;The Journal of Organic Chemistry;2005-06-16
5. Pyramidalized Olefins: A DFT Study of Bicyclo[2.1.1]-, -[3.2.1]-, and -[3.2.2]alkenes and Their Fused Derivatives. Two Rare Examples of π-Facially Symmetric Pyramidal Olefins;The Journal of Organic Chemistry;2004-09-17
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