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A concise, stereoselective synthesis of meso-2,6-diaminopimelic acid (DAP)

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A concise, stereoselective synthesis of meso-2,6-diaminopimelic acid (DAP). / Collier, P N ; Patel, I ; Taylor, R J K .

In: Tetrahedron Letters, Vol. 42, No. 34, 20.08.2001, p. 5953-5954.

Research output: Contribution to journalArticle

Harvard

Collier, PN, Patel, I & Taylor, RJK 2001, 'A concise, stereoselective synthesis of meso-2,6-diaminopimelic acid (DAP)', Tetrahedron Letters, vol. 42, no. 34, pp. 5953-5954.

APA

Collier, P. N., Patel, I., & Taylor, R. J. K. (2001). A concise, stereoselective synthesis of meso-2,6-diaminopimelic acid (DAP). Tetrahedron Letters, 42(34), 5953-5954.

Vancouver

Collier PN, Patel I, Taylor RJK. A concise, stereoselective synthesis of meso-2,6-diaminopimelic acid (DAP). Tetrahedron Letters. 2001 Aug 20;42(34):5953-5954.

Author

Collier, P N ; Patel, I ; Taylor, R J K . / A concise, stereoselective synthesis of meso-2,6-diaminopimelic acid (DAP). In: Tetrahedron Letters. 2001 ; Vol. 42, No. 34. pp. 5953-5954.

Bibtex - Download

@article{7c95b52424e74437ae34b045231035d7,
title = "A concise, stereoselective synthesis of meso-2,6-diaminopimelic acid (DAP)",
abstract = "The preparation of meso-2,6-diaminopimelic acid 1 is described. The key step in the synthesis is Suzuki coupling of the novel organoboron homoalanine equivalent 3 with methyl (2Z)-3-bromo-2-[(tert-butoxycarbonyl)amino]-2-propenoate 5. (C) 2001 Elsevier Science Ltd. All rights reserved.",
keywords = "ASYMMETRIC-SYNTHESIS, AMINO-ACIDS, DIAMINOPIMELIC ACID, DERIVATIVES, INHIBITORS, LYSINE",
author = "Collier, {P N} and I Patel and Taylor, {R J K}",
year = "2001",
month = "8",
day = "20",
language = "English",
volume = "42",
pages = "5953--5954",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "34",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - A concise, stereoselective synthesis of meso-2,6-diaminopimelic acid (DAP)

AU - Collier, P N

AU - Patel, I

AU - Taylor, R J K

PY - 2001/8/20

Y1 - 2001/8/20

N2 - The preparation of meso-2,6-diaminopimelic acid 1 is described. The key step in the synthesis is Suzuki coupling of the novel organoboron homoalanine equivalent 3 with methyl (2Z)-3-bromo-2-[(tert-butoxycarbonyl)amino]-2-propenoate 5. (C) 2001 Elsevier Science Ltd. All rights reserved.

AB - The preparation of meso-2,6-diaminopimelic acid 1 is described. The key step in the synthesis is Suzuki coupling of the novel organoboron homoalanine equivalent 3 with methyl (2Z)-3-bromo-2-[(tert-butoxycarbonyl)amino]-2-propenoate 5. (C) 2001 Elsevier Science Ltd. All rights reserved.

KW - ASYMMETRIC-SYNTHESIS

KW - AMINO-ACIDS

KW - DIAMINOPIMELIC ACID

KW - DERIVATIVES

KW - INHIBITORS

KW - LYSINE

M3 - Article

VL - 42

SP - 5953

EP - 5954

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 34

ER -