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Items: 1 to 20 of 83

1.

Copper-Mediated Nitrosation: 2-Nitrosophenolato Complexes and Their Use in the Synthesis of Heterocycles.

Nicholls AJ, Batsanov AS, Baxendale IR.

Molecules. 2019 Nov 16;24(22). pii: E4154. doi: 10.3390/molecules24224154.

2.

The Synthesis and Utility of Metal-Nitrosophenolato Compounds-Highlighting the Baudisch Reaction.

Nicholls AJ, Barber T, Baxendale IR.

Molecules. 2019 Nov 6;24(22). pii: E4018. doi: 10.3390/molecules24224018. Review.

3.

Flow Hydrodediazoniation of Aromatic Heterocycles.

Röder L, Nicholls AJ, Baxendale IR.

Molecules. 2019 May 24;24(10). pii: E1996. doi: 10.3390/molecules24101996.

4.

A solid-supported arylboronic acid catalyst for direct amidation.

Du Y, Barber T, Lim SE, Rzepa HS, Baxendale IR, Whiting A.

Chem Commun (Camb). 2019 Mar 5;55(20):2916-2919. doi: 10.1039/c8cc09913h.

PMID:
30785133
5.

Synthesis of new derivatives of boehmeriasin A and their biological evaluation in liver cancer.

Güzelcan EA, Baxendale IR, Cetin-Atalay R, Baumann M.

Eur J Med Chem. 2019 Mar 15;166:243-255. doi: 10.1016/j.ejmech.2019.01.056. Epub 2019 Jan 24.

PMID:
30716712
6.

Methyl glycosides via Fischer glycosylation: translation from batch microwave to continuous flow processing.

Aronow J, Stanetty C, Baxendale IR, Mihovilovic MD.

Monatsh Chem. 2019;150(1):11-19. doi: 10.1007/s00706-018-2306-8. Epub 2018 Nov 17.

7.

Indium- and Zinc-Mediated Acyloxyallylation of Protected and Unprotected Aldotetroses-Revealing a Pronounced Diastereodivergence and a Fundamental Difference in the Performance of the Mediating Metal.

Draskovits M, Stanetty C, Baxendale IR, Mihovilovic MD.

J Org Chem. 2018 Mar 2;83(5):2647-2659. doi: 10.1021/acs.joc.7b03063. Epub 2018 Feb 9.

8.

A concise flow synthesis of indole-3-carboxylic ester and its derivatisation to an auxin mimic.

Baumann M, Baxendale IR, Deplante F.

Beilstein J Org Chem. 2017 Nov 29;13:2549-2560. doi: 10.3762/bjoc.13.251. eCollection 2017.

9.

A continuous flow synthesis and derivatization of 1,2,4-thiadiazoles.

Baumann M, Baxendale IR.

Bioorg Med Chem. 2017 Dec 1;25(23):6218-6223. doi: 10.1016/j.bmc.2017.01.022. Epub 2017 Jan 23.

PMID:
28161250
10.

Diastereoselective Trifluoroacetylation of Highly Substituted Pyrrolidines by a Dakin-West Process.

Baumann M, Baxendale IR.

J Org Chem. 2016 Dec 2;81(23):11898-11908. Epub 2016 Nov 17.

PMID:
27934474
11.

Catalytic Chan-Lam coupling using a 'tube-in-tube' reactor to deliver molecular oxygen as an oxidant.

Mallia CJ, Burton PM, Smith AM, Walter GC, Baxendale IR.

Beilstein J Org Chem. 2016 Jul 26;12:1598-607. doi: 10.3762/bjoc.12.156. eCollection 2016.

12.

Flow carbonylation of sterically hindered ortho-substituted iodoarenes.

Mallia CJ, Walter GC, Baxendale IR.

Beilstein J Org Chem. 2016 Jul 19;12:1503-11. doi: 10.3762/bjoc.12.147. eCollection 2016.

13.

Exploring Flow Procedures for Diazonium Formation.

Hu T, Baxendale IR, Baumann M.

Molecules. 2016 Jul 14;21(7). pii: E918. doi: 10.3390/molecules21070918.

14.

Synthesis of 1,3,6-Trisubstituted Azulenes.

Leino TO, Baumann M, Yli-Kauhaluoma J, Baxendale IR, Wallén EA.

J Org Chem. 2015 Nov 20;80(22):11513-20. doi: 10.1021/acs.joc.5b02271. Epub 2015 Nov 11.

PMID:
26528547
15.

Batch and Flow Synthesis of Pyrrolo[1,2-a]-quinolines via an Allene-Based Reaction Cascade.

Baumann M, Baxendale IR.

J Org Chem. 2015 Nov 6;80(21):10806-16. doi: 10.1021/acs.joc.5b01982. Epub 2015 Oct 28.

PMID:
26477591
16.

The synthesis of active pharmaceutical ingredients (APIs) using continuous flow chemistry.

Baumann M, Baxendale IR.

Beilstein J Org Chem. 2015 Jul 17;11:1194-219. doi: 10.3762/bjoc.11.134. eCollection 2015. Review.

17.

Total syntheses of natural products containing spirocarbocycles.

Smith LK, Baxendale IR.

Org Biomol Chem. 2015 Oct 21;13(39):9907-33. doi: 10.1039/c5ob01524c. Review.

PMID:
26356301
18.

Thiazole formation through a modified Gewald reaction.

Mallia CJ, Englert L, Walter GC, Baxendale IR.

Beilstein J Org Chem. 2015 May 26;11:875-83. doi: 10.3762/bjoc.11.98. eCollection 2015.

19.

Large-Scale Synthesis of Crystalline 1,2,3,4,6,7-Hexa-O-acetyl-l-glycero-α-d-manno-heptopyranose.

Stanetty C, Baxendale IR.

European J Org Chem. 2015 Apr;2015(12):2718-2726. Epub 2015 Mar 10.

20.

Flow synthesis of ethyl isocyanoacetate enabling the telescoped synthesis of 1,2,4-triazoles and pyrrolo-[1,2-c]pyrimidines.

Baumann M, Rodriguez Garcia AM, Baxendale IR.

Org Biomol Chem. 2015 Apr 14;13(14):4231-9. doi: 10.1039/c5ob00245a. Epub 2015 Mar 6.

PMID:
25742801

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