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From the same journal

ALPHA-METHOXYKETONE SYNTHESIS VIA KETONE HOMOLOGATION - ZRCL4-MEDIATED HYDROXY SULFONE REARRANGEMENTS

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ALPHA-METHOXYKETONE SYNTHESIS VIA KETONE HOMOLOGATION - ZRCL4-MEDIATED HYDROXY SULFONE REARRANGEMENTS. / MONTANA, J G ; PHILLIPSON, N ; TAYLOR, R J K .

In: JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, No. 19, 07.10.1994, p. 2289-2290.

Research output: Contribution to journalArticle

Harvard

MONTANA, JG, PHILLIPSON, N & TAYLOR, RJK 1994, 'ALPHA-METHOXYKETONE SYNTHESIS VIA KETONE HOMOLOGATION - ZRCL4-MEDIATED HYDROXY SULFONE REARRANGEMENTS', JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, no. 19, pp. 2289-2290.

APA

MONTANA, J. G., PHILLIPSON, N., & TAYLOR, R. J. K. (1994). ALPHA-METHOXYKETONE SYNTHESIS VIA KETONE HOMOLOGATION - ZRCL4-MEDIATED HYDROXY SULFONE REARRANGEMENTS. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, (19), 2289-2290.

Vancouver

MONTANA JG, PHILLIPSON N, TAYLOR RJK. ALPHA-METHOXYKETONE SYNTHESIS VIA KETONE HOMOLOGATION - ZRCL4-MEDIATED HYDROXY SULFONE REARRANGEMENTS. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS. 1994 Oct 7;(19):2289-2290.

Author

MONTANA, J G ; PHILLIPSON, N ; TAYLOR, R J K . / ALPHA-METHOXYKETONE SYNTHESIS VIA KETONE HOMOLOGATION - ZRCL4-MEDIATED HYDROXY SULFONE REARRANGEMENTS. In: JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS. 1994 ; No. 19. pp. 2289-2290.

Bibtex - Download

@article{b2eea55a0fa743a0a4c4d2a617068820,
title = "ALPHA-METHOXYKETONE SYNTHESIS VIA KETONE HOMOLOGATION - ZRCL4-MEDIATED HYDROXY SULFONE REARRANGEMENTS",
abstract = "The adducts between ketones and the anion derived from [(methoxymethyl)sulfonyl]benzene undergo efficient, regioselective rearrangement to give alpha-methoxyketones when treated with ZrCl4 and HfCl4; this new procedure allows the sulfone-mediated homologation methodology to be applied to monocyclic and acyclic ketones.",
keywords = "CARBOHYDRATE-DERIVATIVES, RING EXPANSION",
author = "MONTANA, {J G} and N PHILLIPSON and TAYLOR, {R J K}",
year = "1994",
month = oct,
day = "7",
language = "English",
pages = "2289--2290",
journal = "JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS",
issn = "0022-4936",
publisher = "Chemical Society",
number = "19",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - ALPHA-METHOXYKETONE SYNTHESIS VIA KETONE HOMOLOGATION - ZRCL4-MEDIATED HYDROXY SULFONE REARRANGEMENTS

AU - MONTANA, J G

AU - PHILLIPSON, N

AU - TAYLOR, R J K

PY - 1994/10/7

Y1 - 1994/10/7

N2 - The adducts between ketones and the anion derived from [(methoxymethyl)sulfonyl]benzene undergo efficient, regioselective rearrangement to give alpha-methoxyketones when treated with ZrCl4 and HfCl4; this new procedure allows the sulfone-mediated homologation methodology to be applied to monocyclic and acyclic ketones.

AB - The adducts between ketones and the anion derived from [(methoxymethyl)sulfonyl]benzene undergo efficient, regioselective rearrangement to give alpha-methoxyketones when treated with ZrCl4 and HfCl4; this new procedure allows the sulfone-mediated homologation methodology to be applied to monocyclic and acyclic ketones.

KW - CARBOHYDRATE-DERIVATIVES

KW - RING EXPANSION

M3 - Article

SP - 2289

EP - 2290

JO - JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS

JF - JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS

SN - 0022-4936

IS - 19

ER -