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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 20, 1990 - Issue 22
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Original Articles

5-Bromo-DL-tryptophan and Protected Intermediates for Peptide Synthesis

Noojaree Prasitpan Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, P.O. BOX 6998, m/c 781, Chicago, IL, 60680, USA
,
M. E. Johnson Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, P.O. BOX 6998, m/c 781, Chicago, IL, 60680, USA
&
B. L. Currie Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, P.O. BOX 6998, m/c 781, Chicago, IL, 60680, USA
Pages 3459-3466 | Received 09 Oct 1990, Published online: 24 Oct 2006

Citations (8)

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Read on this site (1)

Dhanapalan Nagarathnam & MichaelE. Johnson. (1993) A New Synthesis of 5-Bromo-DL-tryptophan. Synthetic Communications 23:14, pages 2011-2017.
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Articles from other publishers (7)

Peter Ham, Ben S. Pilgrim & Richard J. G. Simon. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
S. Bittner, R. Scherzer & E. Harlev. (2006) The five bromotryptophans. Amino Acids 33:1, pages 19-42.
Crossref
Peter Ham. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Clarence R. Hurt, Ronghui Lin & Henry Rapoport. (1998) Enantiospecific Synthesis of ( R )-4-Amino-5-oxo-1,3,4,5-tetrahydrobenz[ cd ]indole, an Advanced Intermediate Containing the Tricyclic Core of the Ergots . The Journal of Organic Chemistry 64:1, pages 225-233.
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David Wensbo & Salo Gronowitz. (1996) Indole-3-pyruvic acid oxime ethers and thieno analogues by Heck cyclisation. Application to the synthesis of thia-tryptophans. Tetrahedron 52:47, pages 14975-14988.
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Noojaree Prasitpan, Jayeshkumar N. Patel, Philomen Z. De Croos, Brenda L. Stockwell, Parthasarathy Manavalan, Leela Kar, Michael E. Johnson & Bruce L. Currie. (2009) N‐1 and C‐2 substituted tryptophans as potential inhibitors of sickle cell hemoglobin gelation. Journal of Heterocyclic Chemistry 29:2, pages 335-341.
Crossref
N. PRASITPAN, M. E. JOHNSON & B. L. CURRIE. (2010) ChemInform Abstract: 5‐Bromo‐DL‐tryptophan and Protected Intermediates for Peptide Synthesis.. ChemInform 22:30.
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