Results 1 to 10 of about 2,226,317 (267)

Construction of highly enantioenriched spirocyclopentaneoxindoles containing four consecutive stereocenters via thiourea-catalyzed asymmetric Michael–Henry cascade reactions

open access: yesBeilstein Journal of Organic Chemistry, 2017
The thiourea-catalyzed asymmetric synthesis of highly enantioenriched spirocyclopentaneoxindoles containing chiral amide functional groups using simple 3-substituted oxindoles and nitrovinylacetamide as starting materials was achieved successfully.
Yonglei Du   +5 more
doaj   +1 more source

Synthesis of α-amino amidines through molecular iodine-catalyzed three-component coupling of isocyanides, aldehydes and amines

open access: yesBeilstein Journal of Organic Chemistry, 2014
A facile and efficient synthetic protocol for the synthesis of α-amino amidines has been developed using a molecular iodine-catalyzed three-component coupling reaction of isocyanides, amines, and aldehydes. The presented strategy offers the advantages of
Praveen Reddy Adiyala   +4 more
doaj   +1 more source

Photo-enabled and thioamide-directed α-C(sp3)–H carboxylation of α-substituted benzylamines with CO2 towards α-tertiary amino acids

open access: yesNature Communications
α-Tertiary amino acids (ATAAs) are biologically important molecules that have attracted sustained synthetic interest. However, developing expedient methods for their construction that feature high atom economy and avoid tedious substrate pre ...
Jie Xu   +6 more
doaj   +1 more source

One-pot Ugi-azide and Heck reactions for the synthesis of heterocyclic systems containing tetrazole and 1,2,3,4-tetrahydroisoquinoline

open access: yesBeilstein Journal of Organic Chemistry
A new method for the synthesis of heterocyclic systems containing tetrazole and tetrahydroisoquinoline is developed via the performance of one-pot Ugi-azide and Heck cyclization reactions.
Jiawei Niu   +6 more
doaj   +1 more source

TBAB-catalyzed 1,6-conjugate diazotization of para-quinone methides: A very effective access to polysubstituted α-diazocarbonyl compounds

open access: yesJournal of Saudi Chemical Society
A highly efficient diazotization of diazoacetates with para-quinone methides has been established via a tetrabutyl ammonium bromide (TBAB)-catalyzed 1,6-conjugated addition pathway. This methodology affords a convenient, safe, and rapid way to generating
Zhang-Qin Liu   +2 more
doaj   +1 more source

Synthesis with perfect atom economy: generation of furan derivatives by 1,3-dipolar cycloaddition of acetylenedicarboxylates at cyclooctynes. [PDF]

open access: yesMolecules, 2014
Banert K   +8 more
europepmc   +1 more source

Recent Breakthroughs in Cyclizations of <i>Ortho</i>-Quinone Methides. [PDF]

open access: yesMolecules
Wang D   +5 more
europepmc   +1 more source

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