Donor substituted sulfonyl carbenes, 2: Organothio sulfonyl carbenes
نویسندگان
چکیده
منابع مشابه
Cationic 5-phosphonio-substituted N-heterocyclic carbenes.
2-Phosphanyl-substituted imidazolium salts 2-PR2(4,5-Cl-Im)[OTf] (9a,b[OTf]) (4,5-Cl-Im = 4,5-dichloro-1,3-bis(2,6-di-isopropylphenyl)-imidazolium) (a: R = Cy, b: R = Ph) are prepared from the reaction of R2PCl (R = Cy, Ph) with NHC 8 (4,5-dichloro-1,3-bis(2,6-di-isopropylphenyl)-imidazolin-2-ylidene) in the presence of Me3SiOTf. 5-Phospanyl-substituted imidazolium salts 5-PR2(2,4-Cl-Im)[OTf] (...
متن کاملFlexible cycloalkyl-substituted N-heterocyclic carbenes.
The use of two metal systems cis-Pt(NHC)(2)Me(2) and cis-Ir(NHC)(CO)(2)Cl help to highlight the flexibility of a series of cycloalkyl-substituted N-heterocyclic carbene ligands (ICy, ICy(7), ICy(8), ICy(12)). Bond dissociation enthalpies of several N-heterocyclic carbenes (NHCs) in cis-Pt(NHC)(2)Me(2) are estimated. Electronic and steric parameters of the ICy(n) ligands are quantified and discu...
متن کاملBase-catalyzed cyclization of N-sulfonyl propargylamides to sulfonylmethyl-substituted oxazoles via sulfonyl migration.
The reaction of N-sulfonyl propargylamides in the presence of a base catalyst selectively affords 5-sulfonylmethyl oxazoles via 1,4-sulfonyl migration. Allenes have been established as the key intermediates. Experimental evidence has been provided to support a two-step mechanism in the cyclization.
متن کاملSelective formation of 1,5-substituted sulfonyl triazoles using acetylides and sulfonyl azides.
The reaction of acetylides with sulfonyl azides was found to selectively form 1,5-substituted sulfonyl triazoles. This reaction thus provides access to the regioisomeric product as compared to the popular copper-catalyzed azide-alkyne cycloaddition. The reaction is efficient and selective with a variety of alkyne sources and sulfonyl azides and can incorporate an additional electrophile to yiel...
متن کاملDifferent substituted phenyl carbenes / silylenes/ germylenes: a survey of stability
The effects of halogens; fluorine, chlorine and bromine, on the stability and multiplicity of phenylcarbenes / silylenes/ germylenes structures are compared and contrasted at B3LYP/6-311++G**//B3LYP/6-31+G* level. The singlet-triplet energy gaps, ΔES-T , values for all the above speciesincrease through fluorinated up, ΔES-Ts and ΔEHOMO–LUMOs support the stability of the singlet statesinspite of...
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ژورنال
عنوان ژورنال: Tetrahedron
سال: 1994
ISSN: 0040-4020
DOI: 10.1016/s0040-4020(01)90393-x