Norbornadiene

About: Norbornadiene is a research topic. Over the lifetime, 2389 publications have been published within this topic receiving 38603 citations.

CRC handbook of organic photochemistry and photobiology

Abstract: Photochemistry Cis-Trans Isomerization of Alkenes, J. Saltiel, D.F. Sears, Jr., D.-H. Ko, and K.-M. Park Photorearrangement and Fragmentation of Alkenes, P.J. Kropp (2+2)-Cyclobutane Synthesis (Liquid Phase): Introduction and Mechanistic Consideration, G. Kaupp Cyclobutane Synthesis in the Solid Phase: Introduction and Mechanistic Considerations, G. Kaupp Photochemical Synthesis of Cage Compounds: Propellaprismanes and their Precursors, R. Gleiter and B. Treptow Copper(I) Catalyzed Intra- and Intermolecular Photocycloaddition Reactions of Alkenes, K. Langer and J. Mattay Photoreactions of Alkenes in Protic Media, P.J. Kropp The p-Cyclopropene Rearrangements, H.E. Zimmerman Diene/Cyclobutene Photochemistry, W.J. Leigh Photochemistry of Acyclic 1,3,5-Trienes and Related Compounds, W.H. Laarhoven and H.J.C. Jacobs Photochemistry of Vitamin D and Related Compounds, H.J.C. Jacobs and W.H. Laarhoven Photochemistry of Polyenes Related to Vitamin A, R.S.H. Liu Fulgides and Related Systems, H.G. Heller The Di-p-Methane Rearrangement, H.E. Zimmerman Photorearrangements of Benzobarrelenes and Related Analogues, C.-C. Liao and P.-H. Yang The Photochemistry of Dibenzobarrelene (9,10-Ethenoanthracene) and its Derivatives, J.R. Scheffer and J. Yang Valence Isomerization Between Norbornadiene and Quadricyclane Derivatives-A Solar Energy Storage Process, K. Maruyama and Y. Kubo Ring Isomerization of Benzene and Naphthalene Derivatives, A. Gilbert Phototransposition and Photo-Ring Contraction Reactions of 4-Pyrones and 4-Hydroxypyrylium Cations, J.W. Pavlik Photochemical Aromatic Substitution, J. Cornelisse Photochemical Reactions of Arenes with Amines, N.J. Bunce Intra- and Intermolecular Cycloadditions of Benzene Derivatives, P.A. Wender and T.M. Dore Cyclization of Stilbene and its Derivatives, A. Gilbert Ene Reactions with Singlet Oxygen, A.G. Griesbeck Photooxygenation of 1,3-Dienes, W. Adam and A.G. Griesbeck Photorearrangement of Endope roxides, J. Rigaudy Photochemical Methods for the Synthesis of 1,2-Dioxetanes, A.L. Baumstark and A. Rodriguez Oxidation of Aromatics, A. Albinia and M. Freccero Cyclobutane Photochemistry, K. Mizuno and C. Pac Photochemistry of Oxiranes - Photoreactions of Epoxynaphthoquinones, K. Maruyama and Y. Kubo Photodecarboxylation of Acids and Lactones, P. Wan and D. Budac The Photochemistry of Esters of Carboxylic Acids, J.A. Pincock Carbene Formation in the Photochemistry of Cyclic Ketones, S.M. Roberts Norrish Type I Processes of Ketones: Basic Concepts, C. Bohne Norrish Type I Processes of Ketones: Selected Examples and Synthetic Applications, C. Bohne Photoinduced Intermolecular Hydrogen Abstraction Reactions of Ketones, M. Rubin Hydrogen Abstraction Reactions of a-Diketones, M. Rubin Norrish Type II Photoelimination of Ketones: Cleavage of 1,4-Biradicals Formed by y-Hydrogen Abstraction, .J.-P. Wagner Norrish

A chiral chelating diene as a new type of chiral ligand for transition metal catalysts: its preparation and use for the rhodium-catalyzed asymmetric 1,4-addition.

Abstract: As a new type of chiral ligand, a C2-symmetric norbornadiene derivative (1R,4R)-2,5-dibenzylbicyclo[2.2.1]hepta-2,5-diene (1) was prepared and used for the rhodium-catalyzed asymmetric addition of organoboron and -tin reagents to α,β-unsaturated ketones, which gave high yields of the 1,4-addition products with up to 99% enantioselectivity.

Living Ring-Opening Metathesis Polymerization of 2,3-Difunctionalized- Norbornadienes by Mo(CH-t-Bu)(N-2,6-C(6)H(3)-i-Pr(2)(O-t-Bu)(2)

Abstract: : Benzonorbornadiene 2,3-dicarbomethoxynorbornadiene and 2,3- bis(trifluoromethyl)norbornadiene can be polymerized by Mo(CH-t-Bu)(NAr)(O-t-Bu) 2(Mo(CH-t-Bu)) in a well-behaved living manner to give essentially monodisperse homopolymers. Two of the polymers and (especially) poly 5 are highly trans, and are believed to be tactic. The rate of polymerization is approximately thirty times faster at room temperature, a factor of approximately ten of which can be ascribed to the lower reactivity and the remainder to the lower reactivity relative to 7-Isopropylidene-2-3-dicarbomethoxynorbornadiene is not polymerized at all by Mo(CH-t-Bu), although it does react with Mo(CH-t-Bu). An X-ray structure shows it to be a pseudo-tetrhedral species containing a syn alkylidene ligand (substituent pointing toward the imido nitrogen atom).

A bimetallic hydroformylation catalyst: high regioselectivity and reactivity through homobimetallic cooperativity.

Abstract: The racemic and meso diastereomers of an electron-rich binucleating tetraphosphine ligand have been used to prepare homobimetallic rhodium norbornadiene complexes. The racemic bimetallic Rh complex is an excellent hydroformylation catalyst for 1-alkenes, giving both a high rate of reaction and high regioselectivity for linear aldehydes, whereas the meso complex is considerably slower and less selective. A mechanism involving bimetallic cooperativity between the two rhodium centers in the form of an intramolecular hydride transfer is proposed. Mono- and bimetallic model complexes in which the possibility for bimetallic cooperativity has been reduced or eliminated are very poor catalysts.