J. Castro

发表

Ring-closing metathesis: development of a cyclisation-cleavage strategy for the solid-phase synthesis of cyclic sulfonamides.

Jean-Dominique Moriggi, L. Brown, J. Castro, 2004, Organic & biomolecular chemistry.

Traceless solid phase synthesis of 2,3-disubstituted indoles

C. Swain, J. Castro, G. Stevenson, 1998 .

Total synthesis of (+)-macbecin I

J. Castro, R. Baker, 1990 .

The stereoselectivity of directed aldol reactions with 3-nitro-2-methoxybenzaldehydes is affected by the amine employed as base.

C. Swain, J. Castro, R. Baker, 1988 .

5-HT1E and 5-HT1F receptors

G. Mcallister, J. Castro, 1997 .

Asymmetric synthesis of the northern segment of ephedradine C

R. Ball, N. Tsou, J. Castro, 2000 .

Direct sulfonylation of anilines mediated by visible light† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc03891g

M. Maccoss, C. Schofield, M. Willis, 2017, Chemical science.

Preparation and structure of homochiral tetrahydro-2H-1,3-oxazines

J. Anderson, A. Tabor, A. Aliev, 1999 .

Synthesis of homochiral propargyl amines from N-(Boc)-tetrahydro-2H-1,3-oxazines

A. Tabor, J. Castro, A. Rae, 1999 .

Synthesis of homochiral propargyl amines from tetrahydro-1,3-oxazines

S. Parsons, J. Castro, J. Ker, 1998 .

C−H Cyanation of 6‐Ring N‐Containing Heteroaromatics

M. Maccoss, C. Schofield, M. Willis, 2017, Chemistry.

Total syntheses of justicidin B and retrojusticidin B using a tandem Horner–Emmons–Claisen condensation sequence

M. Bradley, D. Harrowven, J. Castro, 2001 .

Asymmetric synthesis of the northern segment of ephedradine C. A novel dihydrobenzo[b]furan formation

J. Castro, R. Baker, M. G. Russell, 1999 .

Synthesis, biological activity and electrostatic properties of 3-[2-(dimethylamino)ethyl]-5-[(3-amino-1,2,4-thiadiazol-5-yl)methyl]-1H-indole, a novel 5-HT1D receptor agonist.

H. Broughton, V. Matassa, R. Mosley, 1993 .

Rapid analogue synthesis of trisubstituted triazolo[4,3-b]pyridazines

I. Collins, L. Street, J. Castro, 2000 .

Novel lactam NK1 antagonists with anti-emetic activity.

K. Tsao, R. Kilburn, C. Swain, 2006, Bioorganic & medicinal chemistry letters.

4,4-Disubstituted cyclohexylamine NK(1) receptor antagonists II.

K. Tsao, C. Swain, G. Hollingworth, 2002, Bioorganic & medicinal chemistry letters.

A convenient synthesis of highly substituted 2-pyridones

I. Collins, J. Castro, 1999 .

Methiodide approach to the synthesis of 3-[2-(dimethylamino)ethyl]-5-[(1,1-dioxo-5-methyl-1,2,5-thiadiazolidin-2-yl)methyl]-1H-indole and analogues

V. Matassa, J. Castro, 1993 .

Stereoselective construction of the tricyclic core of neoliacinic acid.

J. Castro, W. Whittingham, S. Poigny, 2008, The Journal of organic chemistry.

Synthesis of the Tricyclic Core of the Marine Natural Product Labiatin A

J. Castro, C. Baxter, J. Clark, 2005 .