The diastereoselective Meth-Cohn epoxidation of camphor-derived vinyl sulfones [PDF]
Some camphor-derived vinyl sulfones bearing oxygen functionality at the allylic position have been synthesized and their nucleophilic epoxidation reactions under Meth-Cohn conditions have been explored.
Adam+91 more
core +1 more source
Flexible access to conformationally-locked bicyclic morpholines [PDF]
A preparatively accessible route to a series of conformationally-locked bicyclic morpholines has been developed. This flexible approach allows for diversification in order for a small array of lead-like scaffolds to be synthesised from readily available ...
Brawn+20 more
core +1 more source
Diastereoselective three-component synthesis of beta-amino carbonyl compounds using diazo compounds, boranes, and acyl imines under catalyst-free conditions [PDF]
Diazo compounds, boranes, and acyl imines undergo a three-component Mannich condensation reaction under catalyst-free conditions to give the anti β-amino carbonyl compounds in high diastereoselectivity.
Luan, Yi+4 more
core +1 more source
The cobalt/chromium-catalyzed three-component coupling of aryl iodides, allenes, and aldehydes has been developed to afford multi-substituted homoallylic alcohols in a diastereoselective manner.
Kimihiro Komeyama+4 more
doaj +1 more source
Stereochemical assignment of the protein-protein interaction inhibitor JBIR-22 by total synthesis [PDF]
The authors acknowledge the EPSRC and Cancer Research UK (CRUK Grant No. C21383/A6950) for funding this research.Recent reports have highlighted the biological activity associated with a sub-family of the tetramic acid class of natural products.
Healy, Alan+4 more
core +1 more source
Synthesis of aza-rocaglates via ESIPT-mediated (3+2) photocycloaddition [PDF]
Synthesis of aza-rocaglates, nitrogen-containing analogues of the rocaglate natural products, is reported. The route features ESIPT-mediated (3+2) photocycloaddition of 1-alkyl-2-aryl-3-hydroxyquinolinones with the dipolarophile methyl cinnamate.
Cencic, Regina+4 more
core +1 more source
A diastereoselective approach to the synthesis of berkeleylactone F is presented. The synthetic strategy is initiated with commercially available (R)-glycidol, 1,6-heptadiyne, and (R)-(+)-methyl lactate.
Srijana Subba+2 more
doaj +1 more source
Nickel-Catalyzed Kumada Cross-Coupling Reactions of Benzylic Sulfonamides
Herein, we report a Kumada cross-coupling reaction of benzylic sulfonamides. The scope of the transformation includes acyclic and cyclic sulfonamide precursors that cleanly produce highly substituted acyclic fragments.
Kirsten A. Hewitt+3 more
doaj +1 more source
Terminal substituent effects on the reactivity, thermodynamics, and stereoselectivity of the 8π-6π electrocyclization cascades of 1,3,5,7-tetraenes. [PDF]
M06-2X/6-31+G(d,p) computations are reported for the 8π-6π electrocyclization cascades of 1,3,5,7-tetraenes. The rate-determining step for these cascades is typically the second (6π) ring closure.
Houk, KN, Patel, Ashay
core +2 more sources
Diastereoselective Formation of Complexed Methylenediphosphiranes [PDF]
Stable syn-substituted methylenediphosphirane complexes are obtained from the reaction of transient, electrophilic phosphinidenes [R-P=W(CO)
Jansen, Helen+6 more
openaire +5 more sources