Preparation of L-α-phosphatidyl-D-myo-inositol 3-phosphate (3-PIP) and 3,5-biphosphate (3,5-PIP2)

J. R. Falck; U. Murali Krishna; Jorge H. Capdevila

doi:10.1016/S0960-894X(00)00315-2

Preparation of L-α-phosphatidyl-D-myo-inositol 3-phosphate (3-PIP) and 3,5-biphosphate (3,5-PIP₂)

J. R. Falck, U. Murali Krishna, Jorge H. Capdevila

Biochemistry

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

16 Scopus citations

Abstract

Practical, asymmetric total syntheses of the title phospholipids from a readily available myo-inositol derivative as well as short chain and cross-linkable aminoether analogues are described. (C) 2000 Elsevier Science Ltd. All rights reserved.

Original language	English (US)
Pages (from-to)	1711-1713
Number of pages	3
Journal	Bioorganic and Medicinal Chemistry Letters
Volume	10
Issue number	15
DOIs	https://doi.org/10.1016/S0960-894X(00)00315-2
State	Published - Aug 7 2000

ASJC Scopus subject areas

Biochemistry
Molecular Medicine
Molecular Biology
Pharmaceutical Science
Drug Discovery
Clinical Biochemistry
Organic Chemistry

Access to Document

10.1016/S0960-894X(00)00315-2

Cite this

@article{030ee398da784ab69e7aeeeb27771647,

title = "Preparation of L-α-phosphatidyl-D-myo-inositol 3-phosphate (3-PIP) and 3,5-biphosphate (3,5-PIP2)",

abstract = "Practical, asymmetric total syntheses of the title phospholipids from a readily available myo-inositol derivative as well as short chain and cross-linkable aminoether analogues are described. (C) 2000 Elsevier Science Ltd. All rights reserved.",

author = "Falck, {J. R.} and Krishna, {U. Murali} and Capdevila, {Jorge H.}",

note = "Funding Information: Supported financially by the Robert A. Welch Foundation and NIH (GM31278, GM37922).",

year = "2000",

month = aug,

day = "7",

doi = "10.1016/S0960-894X(00)00315-2",

language = "English (US)",

volume = "10",

pages = "1711--1713",

journal = "Bioorganic and Medicinal Chemistry Letters",

issn = "0960-894X",

publisher = "Elsevier Limited",

number = "15",

}

TY - JOUR

T1 - Preparation of L-α-phosphatidyl-D-myo-inositol 3-phosphate (3-PIP) and 3,5-biphosphate (3,5-PIP2)

AU - Falck, J. R.

AU - Krishna, U. Murali

AU - Capdevila, Jorge H.

N1 - Funding Information: Supported financially by the Robert A. Welch Foundation and NIH (GM31278, GM37922).

PY - 2000/8/7

Y1 - 2000/8/7

N2 - Practical, asymmetric total syntheses of the title phospholipids from a readily available myo-inositol derivative as well as short chain and cross-linkable aminoether analogues are described. (C) 2000 Elsevier Science Ltd. All rights reserved.

AB - Practical, asymmetric total syntheses of the title phospholipids from a readily available myo-inositol derivative as well as short chain and cross-linkable aminoether analogues are described. (C) 2000 Elsevier Science Ltd. All rights reserved.

UR - http://www.scopus.com/inward/record.url?scp=0034618149&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0034618149&partnerID=8YFLogxK

U2 - 10.1016/S0960-894X(00)00315-2

DO - 10.1016/S0960-894X(00)00315-2

M3 - Article

C2 - 10937730

AN - SCOPUS:0034618149

SN - 0960-894X

VL - 10

SP - 1711

EP - 1713

JO - Bioorganic and Medicinal Chemistry Letters

JF - Bioorganic and Medicinal Chemistry Letters

IS - 15

ER -

Preparation of L-α-phosphatidyl-D-myo-inositol 3-phosphate (3-PIP) and 3,5-biphosphate (3,5-PIP₂)

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this