Toward a carbohydrate-based chemistry: progress in the development of general-purpose chiral synthons from carbohydrates
RI Hollingsworth, G Wang - Chemical Reviews, 2000 - ACS Publications
Petroleum is the most used organic resource in the organic chemistry industry, but in many
ways, it is not the ideal chemical feedstock. It is an intractable substance, but thermal …
ways, it is not the ideal chemical feedstock. It is an intractable substance, but thermal …
Synthesis of thiols, selenols, sulfides, selenides, sulfoxides, selenoxides, sulfones and selenones
CM Rayner - Contemporary Organic Synthesis, 1996 - pubs.rsc.org
General methods for sulfoxide and selenoxide synthesis Functionalised sulfoxides and
selenoxides Unsaturated sulfoxides and selenoxides Synthesis of Sulfones and Selenones …
selenoxides Unsaturated sulfoxides and selenoxides Synthesis of Sulfones and Selenones …
3, 5-Bis (trifluoromethyl) phenyl sulfones in the direct Julia− Kocienski olefination
DA Alonso, M Fuensanta, C Nájera… - The Journal of Organic …, 2005 - ACS Publications
3, 5-Bis (trifluoromethyl) phenyl (BTFP) sulfones 7 have been employed in the Julia−
Kocienski olefination reaction with carbonyl compounds. Sulfones 7 are readily prepared in …
Kocienski olefination reaction with carbonyl compounds. Sulfones 7 are readily prepared in …
Access towards enantiopure α, α-difluoromethyl alcohols by means of sulfoxides as traceless chiral auxiliaries
A new methodology to access enantiopure α, α-difluoromethyl alcohols is hereby being
described. The strategy relies on the use of an enantiopure aryl α, α-difluoromethyl sulfoxide …
described. The strategy relies on the use of an enantiopure aryl α, α-difluoromethyl sulfoxide …
3, 5-Bis (trifluoromethyl) phenyl sulfones in the modified Julia olefination: application to the synthesis of resveratrol
DA Alonso, C Nájera, M Varea - Tetrahedron letters, 2004 - Elsevier
The reaction between carbanions derived from alkyl 3, 5-bis (trifluoromethyl) phenyl
sulfones and aldehydes, affords with good yields and stereoselectivities the corresponding …
sulfones and aldehydes, affords with good yields and stereoselectivities the corresponding …
Deprotonation of Benzylic Ethers Using a Hindered Phosphazene Base. A Synthesis of Benzofurans from Ortho-Substituted Benzaldehydes
GA Kraus, N Zhang, JG Verkade, M Nagarajan… - Organic …, 2000 - ACS Publications
Deprotonation of Benzylic Ethers Using a Hindered Phosphazene Base. A Synthesis of
Benzofurans from Ortho-Substituted Benzaldehydes | Organic Letters ACS ACS Publications …
Benzofurans from Ortho-Substituted Benzaldehydes | Organic Letters ACS ACS Publications …
P(RNCH2CH2)3N: Very Strong Non-Ionic Bases Useful in Organic Synthesis
JG Verkade - New Aspects in Phosphorus Chemistry II, 2003 - Springer
Bases of the title type (pro-azaphosphatranes) are very strong (pK a ca. 32 in acetonitrile).
After briefly reviewing recent uses of popular nitrogen-containing bases of various types, the …
After briefly reviewing recent uses of popular nitrogen-containing bases of various types, the …
Synthetic Applications of o- and p-Halobenzyl Sulfones as Zwitterionic Synthons: Preparation of Ortho-Substituted Cinnamates and Biarylacetic Acids
A Costa, C Nájera, JM Sansano - The Journal of Organic …, 2002 - ACS Publications
The synthetic applications of o-halobenzyl and p-halobenzyl sulfones as precursors of 1, 3-
and 1, 5-zwitterionic synthons, respectively, are described. Their α-sulfonyl carbanions …
and 1, 5-zwitterionic synthons, respectively, are described. Their α-sulfonyl carbanions …
Structure and dynamics of α-Aryl Amide and Ketone Enolates: THF, PMDTA, TMTAN, HMPA, and Crypt-Solvated Lithium Enolates, and comparison with …
KJ Kolonko, IA Guzei, HJ Reich - The Journal of Organic …, 2010 - ACS Publications
A variety of multinuclear NMR techniques, in combination with X-ray diffraction methods,
were used to probe the solution structure of α-aryl lithium enolates of bis (4-fluorobenzyl) …
were used to probe the solution structure of α-aryl lithium enolates of bis (4-fluorobenzyl) …
[PDF][PDF] Nucleophilic reactivities of sulfur ylides and related carbanions: Comparison with structurally related organophosphorus compounds
R Appel, H Mayr - Chemistry-a European Journal, 2010 - researchgate.net
Phosphorus and sulfur ylides are two important classes of reagents in organic chemistry.
While phosphorus ylides and related phosphoryl-stabilized carbanions are used in the most …
While phosphorus ylides and related phosphoryl-stabilized carbanions are used in the most …