Zur Synthese von 2.5- und 2.6-verbrückten Tetrahydromethanoindanen

K. Hustert; J. Schmitzer; H. Parlar; F. Korte

doi:10.1515/znb-1979-0333

Zur Synthese von 2.5- und 2.6-verbrückten Tetrahydromethanoindanen

Translated title of the contribution: Synthesis of 2, 5- and 2, 6-Crosslinked Tetrahydromethanoindanes

K. Hustert
, J. Schmitzer
, H. Parlar
, F. Korte

Chair of Food Chemistry and Molecular Sensory Science

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

1 Scopus citations

Abstract

A direct synthetic method for some 2, 5- and 2, 6-crosslinked chlorinated tetrahydromethanoindanes, which are the most important conversion products of cyclodiene insecticides under abiotic conditions, is described. The structures of the resulting compounds are confirmed with the aid of MS and ₁H NMR.

Translated title of the contribution	Synthesis of 2, 5- and 2, 6-Crosslinked Tetrahydromethanoindanes
Original language	German
Pages (from-to)	525-527
Number of pages	3
Journal	Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences
Volume	34
Issue number	3
DOIs	https://doi.org/10.1515/znb-1979-0333
State	Published - 1 Mar 1979

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abstract = "A direct synthetic method for some 2, 5- and 2, 6-crosslinked chlorinated tetrahydromethanoindanes, which are the most important conversion products of cyclodiene insecticides under abiotic conditions, is described. The structures of the resulting compounds are confirmed with the aid of MS and 1H NMR.",

keywords = "Crosslinked Chlorinated Tetrahydromethanoindanes, Cyclodien Insecticides, UV Photolysis",

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AU - Hustert, K.

AU - Schmitzer, J.

AU - Parlar, H.

AU - Korte, F.

PY - 1979/3/1

Y1 - 1979/3/1

N2 - A direct synthetic method for some 2, 5- and 2, 6-crosslinked chlorinated tetrahydromethanoindanes, which are the most important conversion products of cyclodiene insecticides under abiotic conditions, is described. The structures of the resulting compounds are confirmed with the aid of MS and 1H NMR.

AB - A direct synthetic method for some 2, 5- and 2, 6-crosslinked chlorinated tetrahydromethanoindanes, which are the most important conversion products of cyclodiene insecticides under abiotic conditions, is described. The structures of the resulting compounds are confirmed with the aid of MS and 1H NMR.

KW - Crosslinked Chlorinated Tetrahydromethanoindanes

KW - Cyclodien Insecticides

KW - UV Photolysis

UR - https://www.scopus.com/pages/publications/84942967351

U2 - 10.1515/znb-1979-0333

DO - 10.1515/znb-1979-0333

M3 - Artikel

AN - SCOPUS:84942967351

SN - 0932-0776

VL - 34

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JO - Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences

JF - Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences

IS - 3

ER -

Zur Synthese von 2.5- und 2.6-verbrückten Tetrahydromethanoindanen

Abstract

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