A novel synthesis of 3,5-diiodotyrosine with iodic acid

Wangyi Liu; Jianguang Zhou; J. Tze Fei Wong

doi:10.1016/0003-2697(82)90338-4

A novel synthesis of 3,5-diiodotyrosine with iodic acid

Wangyi Liu^*, Jianguang Zhou, J. Tze Fei Wong

^*Corresponding author for this work

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

3 Citations (Scopus)

Abstract

Based on Landolt's reaction between iodic acid and sulfite to produce iodine, a method has been developed for the high-yield iodination of tyrosine to form diiodotyrosine without significant formation of monoiodotyrosine. The use of sulfite as reductant for iodic acid cannot be effectively replaced by citric or oxalic acid under the reaction conditions.

Original language	English
Pages (from-to)	204-207
Number of pages	4
Journal	Analytical Biochemistry
Volume	120
Issue number	1
DOIs	https://doi.org/10.1016/0003-2697(82)90338-4
Publication status	Published - Feb 1982
Externally published	Yes

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@article{bd89c312a3ac45bc929853b36f96bfc7,

title = "A novel synthesis of 3,5-diiodotyrosine with iodic acid",

abstract = "Based on Landolt's reaction between iodic acid and sulfite to produce iodine, a method has been developed for the high-yield iodination of tyrosine to form diiodotyrosine without significant formation of monoiodotyrosine. The use of sulfite as reductant for iodic acid cannot be effectively replaced by citric or oxalic acid under the reaction conditions.",

author = "Wangyi Liu and Jianguang Zhou and Wong, \{J. Tze Fei\}",

year = "1982",

month = feb,

doi = "10.1016/0003-2697(82)90338-4",

language = "English",

volume = "120",

pages = "204--207",

journal = "Analytical Biochemistry",

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publisher = "Academic Press Inc.",

number = "1",

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T1 - A novel synthesis of 3,5-diiodotyrosine with iodic acid

AU - Liu, Wangyi

AU - Zhou, Jianguang

AU - Wong, J. Tze Fei

PY - 1982/2

Y1 - 1982/2

N2 - Based on Landolt's reaction between iodic acid and sulfite to produce iodine, a method has been developed for the high-yield iodination of tyrosine to form diiodotyrosine without significant formation of monoiodotyrosine. The use of sulfite as reductant for iodic acid cannot be effectively replaced by citric or oxalic acid under the reaction conditions.

AB - Based on Landolt's reaction between iodic acid and sulfite to produce iodine, a method has been developed for the high-yield iodination of tyrosine to form diiodotyrosine without significant formation of monoiodotyrosine. The use of sulfite as reductant for iodic acid cannot be effectively replaced by citric or oxalic acid under the reaction conditions.

UR - https://www.webofscience.com/wos/woscc/full-record/WOS:A1982NG36900030

UR - https://www.scopus.com/pages/publications/0019957501

U2 - 10.1016/0003-2697(82)90338-4

DO - 10.1016/0003-2697(82)90338-4

M3 - Journal Article

C2 - 7091654

AN - SCOPUS:0019957501

SN - 0003-2697

VL - 120

SP - 204

EP - 207

JO - Analytical Biochemistry

JF - Analytical Biochemistry

IS - 1

ER -

A novel synthesis of 3,5-diiodotyrosine with iodic acid

Abstract

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