Tin-mediated CH activation and cross-coupling in a single flask

Jeffrey M. Bartolin; Ajdin Kavara; Jeff Kampf; Mark M. Banaszak Holl

doi:10.1021/om060388s

Tin-mediated CH activation and cross-coupling in a single flask

Jeffrey M. Bartolin, Ajdin Kavara, Jeff Kampf, Mark M. Banaszak Holl

Chemical & Biological Engineering

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

35 Citations (Scopus)

Abstract

Tin-mediated CH activation and cross-coupling in a single flask has been achieved by employing a mixed stannylene/phenyl iodide reagent followed by Stille cross-coupling. The reagent has been successfully employed for alkanes and ethers and shows radical-like regioselectivity.

Original language	English
Pages (from-to)	4738-4740
Number of pages	3
Journal	Organometallics
Volume	25
Issue number	20
DOIs	https://doi.org/10.1021/om060388s
Publication status	Published - 25 Sept 2006

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10.1021/om060388s

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title = "Tin-mediated CH activation and cross-coupling in a single flask",

abstract = "Tin-mediated CH activation and cross-coupling in a single flask has been achieved by employing a mixed stannylene/phenyl iodide reagent followed by Stille cross-coupling. The reagent has been successfully employed for alkanes and ethers and shows radical-like regioselectivity.",

author = "Bartolin, \{Jeffrey M.\} and Ajdin Kavara and Jeff Kampf and \{Banaszak Holl\}, \{Mark M.\}",

year = "2006",

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T1 - Tin-mediated CH activation and cross-coupling in a single flask

AU - Bartolin, Jeffrey M.

AU - Kavara, Ajdin

AU - Kampf, Jeff

AU - Banaszak Holl, Mark M.

PY - 2006/9/25

Y1 - 2006/9/25

N2 - Tin-mediated CH activation and cross-coupling in a single flask has been achieved by employing a mixed stannylene/phenyl iodide reagent followed by Stille cross-coupling. The reagent has been successfully employed for alkanes and ethers and shows radical-like regioselectivity.

AB - Tin-mediated CH activation and cross-coupling in a single flask has been achieved by employing a mixed stannylene/phenyl iodide reagent followed by Stille cross-coupling. The reagent has been successfully employed for alkanes and ethers and shows radical-like regioselectivity.

UR - https://www.scopus.com/pages/publications/33749822682

U2 - 10.1021/om060388s

DO - 10.1021/om060388s

M3 - Article

AN - SCOPUS:33749822682

SN - 0276-7333

VL - 25

SP - 4738

EP - 4740

JO - Organometallics

JF - Organometallics

IS - 20

ER -

Tin-mediated CH activation and cross-coupling in a single flask

Abstract

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