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Ring expansion and contraction
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the contraction. The standard intermediates are anionic, cationic, and carbenoid. The Favorskii rearrangement is a classic anionic ring contraction. ItBuchner ring expansion (1,722 words) [view diff] exact match in snippet view article find links to article
highly explosive nature of diazoacetic esters. Preparation of the metal carbenoid: Synthesis of the carbene in the 1960s was focused on using copper catalystsBisoxazoline ligand (2,222 words) [view diff] exact match in snippet view article find links to article
reactions, this began with the very first application of BOX ligands in carbenoid cyclopropanations and has been expanded to include 1,3-Dipolar cycloadditionSchiff base (869 words) [view diff] exact match in snippet view article find links to article
1968 Ryōji Noyori developed a copper-Schiff base complex for the metal-carbenoid cyclopropanation of styrene. Schiff bases have also been incorporatedLombardo methylenation (354 words) [view diff] exact match in snippet view article find links to article
Jianfeng; Main, Calver A.; McKiernan, Gordon J. (2007-06-04). "Titanium carbenoid reagents for converting carbonyl groups into alkenes". Tetrahedron. 63Tebbe's reagent (907 words) [view diff] exact match in snippet view article find links to article
Li, Jianfeng; Main, Calver A.; McKiernan, Gordon J. (2007). "Titanium carbenoid reagents for converting carbonyl groups into alkenes". Tetrahedron. 63Huw Davies (chemist) (197 words) [view diff] exact match in snippet view article
synthesis and drug discovery. His program covers design of chiral catalysts, carbenoid chemistry, development of new synthetic methodology, total synthesis ofCascade reaction (2,825 words) [view diff] exact match in snippet view article find links to article
Treatment of diazoimide 64 with rhodium(II) acetate dimer generated a carbenoid that yielded reactive ylide 65 after an intramolecular cyclization withTransition metal formyl complex (374 words) [view diff] exact match in snippet view article find links to article
motivated by interest in Fischer-Tropsch chemistry. O-alkylation gives carbenoid complexes. The formyl ligand also functions as a base, allowing the formation1,3-Dipolar cycloaddition (6,426 words) [view diff] exact match in snippet view article find links to article
characterization of stable ruthenium-carbenoid complexes and rhodium metallocarbenes, involves an initial formation of a metal-carbenoid complex from the diazo compoundPetasis reagent (396 words) [view diff] exact match in snippet view article find links to article
Hartley, R. C.; Li, J.; Main, C. A.; McKiernan, G. J. (2007). "Titanium carbenoid reagents for converting carbonyl groups into alkenes". Tetrahedron. 63Bamford–Stevens reaction (1,481 words) [view diff] exact match in snippet view article find links to article
1021/ja028020j. PMID 12381180. Wood, J. (1999). "Development of a Rhodium Carbenoid-Initiated Claisen Rearrangement for the Enantioselective Synthesis ofVinylidene group (313 words) [view diff] exact match in snippet view article find links to article
DDT-derived vinylidene complex Fe(TPP)C2(C6H4Cl)2, one of several iron carbenoid complexes prepared by Mansuy (TPP = conjugate base of tetraphenylporphyrin)Enantioselective synthesis (4,718 words) [view diff] exact match in snippet view article find links to article
complex using a chiral Schiff base ligand, which he used for the metal–carbenoid cyclopropanation of styrene. In common with Knowles' findings, Noyori'sAlkyne trimerisation (1,917 words) [view diff] exact match in snippet view article find links to article
metallanorbornadienes, and a more complicated structure featuring a carbenoid ligand. Catalysts used include cyclopentadienylcobalt dicarbonyl and Wilkinson'sDoering–LaFlamme allene synthesis (395 words) [view diff] exact match in snippet view article find links to article
Doering–LaFlamme allene synthesis with enantiopure cyclopropylmagnesium carbenoids". Tetrahedron Letters. 52 (23): 3016–3019. doi:10.1016/j.tetlet.2011.03Organotitanium chemistry (1,866 words) [view diff] exact match in snippet view article find links to article
Li, Jianfeng; Main, Calver A.; McKiernan, Gordon J. (2007). "Titanium carbenoid reagents for converting carbonyl groups into alkenes". Tetrahedron. 63Wendy Young (663 words) [view diff] exact match in snippet view article find links to article
Davies. She was co-author on an early application of Davies' rhodium(II) carbenoid insertion - Cope rearrangement chemistry, leading to the total synthesisDoyle–Kirmse reaction (541 words) [view diff] exact match in snippet view article find links to article
nickel. Modifications using other carbenes are reported e.g. (2-furyl)carbenoids. The reaction is not strictly limited to allyl compounds. Propargyl-sulfideTetraphenylporphyrin (948 words) [view diff] exact match in snippet view article find links to article
= amide groups). Structure of Fe(TPP)CC(C6H4Cl)2, one of several iron carbenoid complexes reported by Daniel Mansuy. Sulfonated derivatives of TPP areBase-promoted epoxide isomerization (1,120 words) [view diff] exact match in snippet view article find links to article
allylic alcohols are formed from these substrates without competitive carbenoid transformations. The use of bulky aluminum amide bases facilitates eliminationDaniel Mansuy (483 words) [view diff] exact match in snippet view article find links to article
Structure of Fe(TPP)C2(C6H4Cl)2, one of several iron carbenoid complexes prepared by Mansuy (TPP = conjugate base of tetraphenylporphyrin).Transition metal carbene complex (1,966 words) [view diff] exact match in snippet view article find links to article
and sometimes π-donor metal ligands hydrogen and alkyl substituents on carbenoid carbon. Examples include ((CH3)3CCH2)Ta=CHC(CH3)3 and Os(PPh3)2(NO)Cl(=CH2)Total synthesis of morphine and related alkaloids (948 words) [view diff] exact match in snippet view article find links to article
1999). "Asymmetric Total Synthesis of (+)-Codeine via Intramolecular Carbenoid Insertion". The Journal of Organic Chemistry. 64 (21): 7871–7884. doi:10Olefin metathesis (4,093 words) [view diff] exact match in snippet view article find links to article
imido ligands. Grubbs catalysts, on the other hand, are ruthenium(II) carbenoid complexes. Many variations of Grubbs catalysts are known. Some have beenFrank Westheimer (3,571 words) [view diff] exact match in snippet view article find links to article
enabled it to react with the enzyme. The photolabel generated a reactive carbenoid species capable of inserting into hydrocarbon C-H bonds. Westheimer alsoSchwartz's reagent (1,662 words) [view diff] exact match in snippet view article find links to article
of Crotylsilanes Accessed by Enantioselective Rh(II) or Cu(I) Promoted Carbenoid Si–H Insertion". J. Org. Chem. 76 (24): 9900–9918. doi:10.1021/jo202119pBioconjugation (4,661 words) [view diff] exact match in snippet view article find links to article
reactions. Rh-catalyzed Trp and Cys alkylation Using in situ generated RhII-carbenoid by activation of vinyl-substituted diazo compounds with Rh2(OAc)4, tryptophansPropellane (2,470 words) [view diff] exact match in snippet view article find links to article
doi:10.1021/ja00449a045. Hamon, David P. G.; Trenerry, V. Craige (1981). "Carbenoid insertion reactions: formation of [4.1.1]propellane". J. Am. Chem. SocElias James Corey (5,524 words) [view diff] exact match in snippet view article find links to article
thionocarbonate and trialkylphosphite either form a phosphorus ylide or carbenoid intermediate. The reaction is stereospecific for most substrates unlessGuy Bertrand (chemist) (1,554 words) [view diff] exact match in snippet view article
Igau, H. Grutzmacher, A. Baceiredo, G. Bertrand, « Analogous a, a' bis carbenoid triply bonded species : synthesis of a stable l 3-phosphinocarbene _lCycloisomerization (1,714 words) [view diff] exact match in snippet view article find links to article
2–shift of the propargyl ester mediated by Au to give a syn–Au vinyl carbenoid species (29). Computational studies show that the syn–intermediate, 29Morphine (13,643 words) [view diff] exact match in snippet view article find links to article
1999). "Asymmetric Total Synthesis of (+)-Codeine via Intramolecular Carbenoid Insertion". The Journal of Organic Chemistry. 64 (21): 7871–7884. doi:10Persistent carbene (6,933 words) [view diff] exact match in snippet view article find links to article
H. Grutzmacher; A. Baceiredo; G. Bertrand (1988). "Analogous α,α′-bis-carbenoid, triply bonded species: synthesis of a stable λ3-phosphino carbene-λ3-phosphaacetylene"