The addition of allyllioronates to sulfenimines gives homoallylsulfenamides which are potentially versatile Intermediates for alkaloid synthesis.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/26462/1/0000550.pd
A chiral rhodium complex catalyzes the highly enantioselective coupling of arylboronic acids, 1,3-en...
In the following thesis, new methodologies which exploit sulfinylamine reagents to enable one-pot sy...
Chalcogenides are highly redox active and biologically potent nucleophiles with significant unexplor...
The ever-increasing prevalence of sulfoximine derivatives in drug discovery programmes has brought a...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
The reaction of allylboronates with sulfenimines, aldimines and aldoximes has been systematically ex...
Organocatalysts have been a hot area of exploration, due to both concept novelty and significant rea...
The highly strained γ-sultine 4, resulting from the addition of SO2 to benzobenzvalene, is shown to ...
The development of new methods to skeletally diverse sultams based on a central α-halo benzene sulfo...
The indium-promoted allylation of chiral N-sulfinyl imines represents a useful and versatile procedu...
Au cours de ces trente dernières années, les allylboranes, une classe particulière de composés organ...
Direct synthesis of NH-sulfoximines from sulfides has been achieved through O and NH transfer in the...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...
International audience2-Sulfonimidoylylidene tetrahydrofurans and 2-sulfonimidoylylidene-5-vinyl tet...
This thesis is divided into three chapters. Chapter 1 provides brief reviews on the subjects of pre...
A chiral rhodium complex catalyzes the highly enantioselective coupling of arylboronic acids, 1,3-en...
In the following thesis, new methodologies which exploit sulfinylamine reagents to enable one-pot sy...
Chalcogenides are highly redox active and biologically potent nucleophiles with significant unexplor...
The ever-increasing prevalence of sulfoximine derivatives in drug discovery programmes has brought a...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
The reaction of allylboronates with sulfenimines, aldimines and aldoximes has been systematically ex...
Organocatalysts have been a hot area of exploration, due to both concept novelty and significant rea...
The highly strained γ-sultine 4, resulting from the addition of SO2 to benzobenzvalene, is shown to ...
The development of new methods to skeletally diverse sultams based on a central α-halo benzene sulfo...
The indium-promoted allylation of chiral N-sulfinyl imines represents a useful and versatile procedu...
Au cours de ces trente dernières années, les allylboranes, une classe particulière de composés organ...
Direct synthesis of NH-sulfoximines from sulfides has been achieved through O and NH transfer in the...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...
International audience2-Sulfonimidoylylidene tetrahydrofurans and 2-sulfonimidoylylidene-5-vinyl tet...
This thesis is divided into three chapters. Chapter 1 provides brief reviews on the subjects of pre...
A chiral rhodium complex catalyzes the highly enantioselective coupling of arylboronic acids, 1,3-en...
In the following thesis, new methodologies which exploit sulfinylamine reagents to enable one-pot sy...
Chalcogenides are highly redox active and biologically potent nucleophiles with significant unexplor...
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