Axial-selectivity in prins cyclization reaction: Synthesis of 4-iodotetrahydropyrans

Anil K. Saikia; Somasekhar Bondalapati; Kiran Indukuri; Paramartha Gogoi

doi:10.1246/cl.2011.1176

Axial-selectivity in prins cyclization reaction: Synthesis of 4-iodotetrahydropyrans

Anil K. Saikia, Somasekhar Bondalapati, Kiran Indukuri, Paramartha Gogoi

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

8 Scopus citations

Abstract

Trimethylsily1 triflate and tetrabutylammonium iodide (TBAI) effectively mediate the Prins cyclization of homoallylic alcohols and aldehydes to give 4-iodotetrahydropyrans with axial selectivity and good yields.

Original language	English
Pages (from-to)	1176-1178
Number of pages	3
Journal	Chemistry Letters
Volume	40
Issue number	10
DOIs	https://doi.org/10.1246/cl.2011.1176
State	Published - 1 Dec 2011
Externally published	Yes

ASJC Scopus subject areas

General Chemistry

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title = "Axial-selectivity in prins cyclization reaction: Synthesis of 4-iodotetrahydropyrans",

abstract = "Trimethylsily1 triflate and tetrabutylammonium iodide (TBAI) effectively mediate the Prins cyclization of homoallylic alcohols and aldehydes to give 4-iodotetrahydropyrans with axial selectivity and good yields.",

author = "Saikia, {Anil K.} and Somasekhar Bondalapati and Kiran Indukuri and Paramartha Gogoi",

year = "2011",

month = dec,

day = "1",

doi = "10.1246/cl.2011.1176",

language = "English",

volume = "40",

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journal = "Chemistry Letters",

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publisher = "Oxford University Press",

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T1 - Axial-selectivity in prins cyclization reaction

T2 - Synthesis of 4-iodotetrahydropyrans

AU - Saikia, Anil K.

AU - Bondalapati, Somasekhar

AU - Indukuri, Kiran

AU - Gogoi, Paramartha

PY - 2011/12/1

Y1 - 2011/12/1

N2 - Trimethylsily1 triflate and tetrabutylammonium iodide (TBAI) effectively mediate the Prins cyclization of homoallylic alcohols and aldehydes to give 4-iodotetrahydropyrans with axial selectivity and good yields.

AB - Trimethylsily1 triflate and tetrabutylammonium iodide (TBAI) effectively mediate the Prins cyclization of homoallylic alcohols and aldehydes to give 4-iodotetrahydropyrans with axial selectivity and good yields.

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U2 - 10.1246/cl.2011.1176

DO - 10.1246/cl.2011.1176

M3 - Article

AN - SCOPUS:84861954579

SN - 0366-7022

VL - 40

SP - 1176

EP - 1178

JO - Chemistry Letters

JF - Chemistry Letters

IS - 10

ER -

Axial-selectivity in prins cyclization reaction: Synthesis of 4-iodotetrahydropyrans

Abstract

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