Synthesis of orthogonally protected L-homocysteine and L-2-amino-4-phophonobutanoic acid from L-homoserine

S. A. Nair; B. Lee; D. G. Hangauer

doi:10.1055/s-1995-4015

Synthesis of orthogonally protected L-homocysteine and L-2-amino-4-phophonobutanoic acid from L-homoserine

S. A. Nair
, B. Lee
, D. G. Hangauer

Chemistry

University at Buffalo

SUNY Buffalo

Research output: Contribution to journal › Article › peer-review

16 Scopus citations

Abstract

Convenient syntheses of N-tert-butoxycarbonyl-S-p-methoxybenzyl-L-homocysteine benzyl ester and benzyl L-4-dimethylphosphono-2-N-phthalimidobutanoate from commercially available L-homoserine are described along with their incorporation into dipeptides.

Original language	English
Pages (from-to)	810-814
Number of pages	5
Journal	Synthesis (Germany)
Issue number	7
DOIs	https://doi.org/10.1055/s-1995-4015
State	Published - 1995

Keywords

L-2-amino-4- bromobutyrate
L-2-amino-4-phosphonobutyrate
L-homocysteine
L-homoserine

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10.1055/s-1995-4015

Cite this

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title = "Synthesis of orthogonally protected L-homocysteine and L-2-amino-4-phophonobutanoic acid from L-homoserine",

abstract = "Convenient syntheses of N-tert-butoxycarbonyl-S-p-methoxybenzyl-L-homocysteine benzyl ester and benzyl L-4-dimethylphosphono-2-N-phthalimidobutanoate from commercially available L-homoserine are described along with their incorporation into dipeptides.",

keywords = "L-2-amino-4- bromobutyrate, L-2-amino-4-phosphonobutyrate, L-homocysteine, L-homoserine",

author = "Nair, \{S. A.\} and B. Lee and Hangauer, \{D. G.\}",

year = "1995",

doi = "10.1055/s-1995-4015",

language = "English",

pages = "810--814",

journal = "Synthesis (Germany)",

issn = "0039-7881",

publisher = "Georg Thieme Verlag",

number = "7",

}

TY - JOUR

T1 - Synthesis of orthogonally protected L-homocysteine and L-2-amino-4-phophonobutanoic acid from L-homoserine

AU - Nair, S. A.

AU - Lee, B.

AU - Hangauer, D. G.

PY - 1995

Y1 - 1995

N2 - Convenient syntheses of N-tert-butoxycarbonyl-S-p-methoxybenzyl-L-homocysteine benzyl ester and benzyl L-4-dimethylphosphono-2-N-phthalimidobutanoate from commercially available L-homoserine are described along with their incorporation into dipeptides.

AB - Convenient syntheses of N-tert-butoxycarbonyl-S-p-methoxybenzyl-L-homocysteine benzyl ester and benzyl L-4-dimethylphosphono-2-N-phthalimidobutanoate from commercially available L-homoserine are described along with their incorporation into dipeptides.

KW - L-2-amino-4- bromobutyrate

KW - L-2-amino-4-phosphonobutyrate

KW - L-homocysteine

KW - L-homoserine

UR - https://www.scopus.com/pages/publications/0029145056

U2 - 10.1055/s-1995-4015

DO - 10.1055/s-1995-4015

M3 - Article

SN - 0039-7881

SP - 810

EP - 814

JO - Synthesis (Germany)

JF - Synthesis (Germany)

IS - 7

ER -

Synthesis of orthogonally protected L-homocysteine and L-2-amino-4-phophonobutanoic acid from L-homoserine

Abstract

Keywords

Access to Document

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