Dehydrogenation of diamine-monoboranes to cyclic diaminoboranes: An efficient catalyzed dehydrogenative cyclization (CDC)

Christopher Wallis; H. Dyer; L. Vendier; G. Alcaraz; S. Sabo-Etienne

doi:10.1002/anie.201108874

Dehydrogenation of diamine-monoboranes to cyclic diaminoboranes: An efficient catalyzed dehydrogenative cyclization (CDC)

Christopher Wallis, H. Dyer, L. Vendier, G. Alcaraz, S. Sabo-Etienne

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

Abstract

Remote control: The title reaction is the first example of a catalyzed dehydrogenative cyclization (CDC) of diamine–monoboranes to give cyclic diaminoboranes. The cyclization reaction is strongly dependent on the nature of the substitution pattern at the remote amino group.

Original language	English
Pages (from-to)	3646-3648
Journal	Angewandte Chemie International Edition
Volume	51
Issue number	15
DOIs	https://doi.org/10.1002/anie.201108874
Publication status	Published - 15 Feb 2012
Externally published	Yes

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10.1002/anie.201108874

Cite this

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title = "Dehydrogenation of diamine-monoboranes to cyclic diaminoboranes: An efficient catalyzed dehydrogenative cyclization (CDC)",

abstract = "Remote control: The title reaction is the first example of a catalyzed dehydrogenative cyclization (CDC) of diamine–monoboranes to give cyclic diaminoboranes. The cyclization reaction is strongly dependent on the nature of the substitution pattern at the remote amino group.",

author = "Christopher Wallis and {H. Dyer} and {L. Vendier} and {G. Alcaraz} and {S. Sabo-Etienne}",

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AU - Wallis, Christopher

AU - H. Dyer

AU - L. Vendier

AU - G. Alcaraz

AU - S. Sabo-Etienne

PY - 2012/2/15

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N2 - Remote control: The title reaction is the first example of a catalyzed dehydrogenative cyclization (CDC) of diamine–monoboranes to give cyclic diaminoboranes. The cyclization reaction is strongly dependent on the nature of the substitution pattern at the remote amino group.

AB - Remote control: The title reaction is the first example of a catalyzed dehydrogenative cyclization (CDC) of diamine–monoboranes to give cyclic diaminoboranes. The cyclization reaction is strongly dependent on the nature of the substitution pattern at the remote amino group.

U2 - 10.1002/anie.201108874

DO - 10.1002/anie.201108874

M3 - Article

SN - 1433-7851

VL - 51

SP - 3646

EP - 3648

JO - Angewandte Chemie International Edition

JF - Angewandte Chemie International Edition

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