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Longer titles found: Diazoalkane 1,3-dipolar cycloaddition (view)

searching for 1,3-Dipolar cycloaddition 16 found (74 total)

Click chemistry (5,477 words) [view diff] case mismatch in snippet view article find links to article

Existing reactions, such as Staudinger ligation and the Huisgen 1,3-dipolar cycloaddition, have been modified and optimized for such reaction conditions
Isoindoline (273 words) [view diff] case mismatch in snippet view article find links to article
Isoindolines via One-Pot Sequential Cu(I)-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition/Aromatization DOI: 10.1021/ol302987h Asymmetric organocatalytic
Acyl cyanide (408 words) [view diff] case mismatch in snippet view article find links to article
(2002). "A Click Chemistry Approach to Tetrazoles by Huisgen 1,3-Dipolar Cycloaddition: Synthesis of 5-Acyltetrazoles from Azides and Acyl Cyanides"
Tributyltin azide (185 words) [view diff] case mismatch in snippet view article find links to article
blisters. Aureggi, Valentina; Sedelmeier, Gottfried (2007). "1,3-Dipolar Cycloaddition: Click Chemistry for the Synthesis of 5-Substituted Tetrazoles
Triazole (1,024 words) [view diff] case mismatch in snippet view article find links to article
technique for unsubstituted triazoles is the Huisgen azide-alkyne 1,3-dipolar cycloaddition: a azide and an alkyne react at high temperature to form a ring
3-Azidocoumarin (368 words) [view diff] case mismatch in snippet view article find links to article
Press: San Diego, 1996. Q. Wang; et al. (2004). "A Fluorogenic 1,3-Dipolar Cycloaddition Reaction of 3-Azidocoumarins and Acetylenes". Org. Lett. 6 (24):
Activity-based proteomics (536 words) [view diff] case mismatch in snippet view article find links to article
such as biotin or an alkyne or azide for use with the Huisgen 1,3-dipolar cycloaddition (also known as click chemistry). A major advantage of ABPP is
Adam S. Veige (945 words) [view diff] exact match in snippet view article find links to article
Castillo, T. J.; Sarkar, S.; Abboud, K. A.; Veige, A. S. (2011). "1,3-Dipolar cycloaddition between a metal–azide (Ph3PAuN3) and a metal–acetylide (Ph3PAuC≡CPh):
Reactivity (chemistry) (1,202 words) [view diff] case mismatch in snippet view article
K. N. (2007-08-09). "Distortion/Interaction Energy Control of 1,3-Dipolar Cycloaddition Reactivity". Journal of the American Chemical Society. 129 (35):
Flavin prenyltransferase (UbiX) (765 words) [view diff] case mismatch in snippet view article
"New cofactor supports α,β-unsaturated acid decarboxylation via 1,3-dipolar cycloaddition". Nature. 522 (7557): 497–501. Bibcode:2015Natur.522..497P. doi:10
Prenylated flavin mononucleotide (491 words) [view diff] case mismatch in snippet view article find links to article
"New cofactor supports α,β-unsaturated acid decarboxylation via 1,3-dipolar cycloaddition". Nature. 522 (7557): 497–501. Bibcode:2015Natur.522..497P. doi:10
Affinity label (1,176 words) [view diff] case mismatch in snippet view article find links to article
such as biotin or an alkyne or azide for use with the Huisgen 1,3-dipolar cycloaddition (also known as click chemistry). Suicide inhibition Wofsy L, Metzger
Sam Hay (chemist) (922 words) [view diff] case mismatch in snippet view article
"New cofactor supports α,β-unsaturated acid decarboxylation via 1,3-dipolar cycloaddition". Nature. 522 (7557): 497–501. Bibcode:2015Natur.522..497P. doi:10
Muscimol (2,481 words) [view diff] case mismatch in snippet view article find links to article
Napoletano M, Sala A (1986). "A convenient synthesis of muscimol by a 1,3-dipolar cycloaddition reaction". Tetrahedron Letters. 27 (27): 3181–3182. doi:10
Elias James Corey (5,524 words) [view diff] case mismatch in snippet view article find links to article
doi:10.1021/jo970907o. Nair; et al. (2007). "Intramolecular 1,3-dipolar cycloaddition reactions in targeted syntheses". Tetrahedron. 63 (50): 12247–12275
Aldehyde tag (2,916 words) [view diff] case mismatch in snippet view article find links to article
the copper-free click chemistry was selected. A strain-promoted 1,3-dipolar cycloaddition of a cyclooctynes and an azide was carried out forming a covalent