Results 81 to 90 of about 66,905 (286)

Synthesis of Conjugated Linear and Cyclic Polyynes by Selective Alkyne Metathesis. [PDF]

open access: yesAngew Chem Int Ed Engl
The formation of polyynes with an odd number of conjugated triple bonds is challenging, particularly for complex architectures since most established methods rely on irreversible C–C bond‐forming reactions. To address this, we have developed the synthesis of triynes via alkyne metathesis.
Escudero J   +12 more
europepmc   +3 more sources

Metathesis Reactions of Carbohydrates: Recent Highlights in Cross‐Metathesis

open access: yesEuropean Journal of Organic Chemistry, 2010
AbstractMetathetical processes play a prominent role in the development of useful transformations because of their mildness, tolerance of functional groups, and synthetic potential. On the other hand, carbohydrates have gained well‐deserved relevance in the study of biological processes.
Aljarilla, Ana   +2 more
openaire   +2 more sources

Bidentate N,O-prolinate ruthenium benzylidene catalyst highly active in RCM of disubstituted dienes [PDF]

open access: yes, 2007
The synthesis of a bidentate N,O-prolinate ruthenium benzylidene from commercially available starting materials and its activity in ring-closing metathesis of functionalized disubstituted dienes at 30 °C is ...
Grubbs, Robert H., Samec, Joseph S. M.
core   +3 more sources

Light-induced olefin metathesis

open access: yesBeilstein Journal of Organic Chemistry, 2010
Light activation is a most desirable property for catalysis control. Among the many catalytic processes that may be activated by light, olefin metathesis stands out as both academically motivating and practically useful.
Yuval Vidavsky, N. Gabriel Lemcoff
doaj   +1 more source

First Total Synthesis of Cryptopyranmoscatone A3 and Crypto­pyranmoscatone B4

open access: yesSynOpen, 2018
The first total synthesis of cryptopyranmoscatones A3 and B4 has been accomplished from d-ribose or but-3-ynol. The key steps involved in the synthesis are oxa-Michael addition, highly diastereo­selective Brown allylation, and ring closing metathesis ...
A. Maheswara Reddy, Gowravaram Sabitha
doaj   +1 more source

Olefin metathesis in multiblock copolymer synthesis

open access: yesBeilstein Journal of Organic Chemistry, 2019
Multiblock copolymers constitute a basis for an emerging class of nanomaterials that combine various functional properties with durability and enhanced mechanical characteristics. Our mini-review addresses synthetic approaches to the design of multiblock
Maria L. Gringolts   +3 more
doaj   +1 more source

Functionalized hyperbranched polymers via olefin metathesis [PDF]

open access: yes, 2009
Hyperbranched polymers are highly branched, three-dimensional macromolecules which are closely related to dendrimers and are typically prepared via a one-pot polycondensation of AB_(n≥2) monomers.^1 Although hyperbranched macromolecules lack the ...
Gorodetskaya, Irina A.   +3 more
core   +1 more source

Conformations of N-Heterocyclic Carbene Ligands in Ruthenium Complexes Relevant to Olefin Metathesis [PDF]

open access: yes, 2009
The structure of ruthenium-based olefin metathesis catalyst 3 and model π-complex 5 in solution and in the solid state are reported. The N-tolyl ligands, due to their lower symmetry than the traditional N-mesityl substituents, complicate this analysis ...
Benitez, Diego   +6 more
core   +3 more sources

Cyclization Strategies in Carbonyl–Olefin Metathesis: An Up-to-Date Review

open access: yesMolecules
The metathesis reaction between carbonyl compounds and olefins has emerged as a potent strategy for facilitating swift functional group interconversion and the construction of intricate organic structures through the creation of novel carbon–carbon ...
Xiaoke Zhang
doaj   +1 more source

Formation of bridged bicycloalkenes via ring closing metathesis [PDF]

open access: yes, 1998
Ring closing metathesis may be used in the formation of small ring bicycloalkenes from monocyclic diene ...
Grubbs, Robert H., Morehead, Andrew, Jr.
core   +1 more source

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