Doping-addition of arylsulfenyl chlorides to the tricyclo[4,2,2,02,5]deca-3,7,9-triene system: skeletal rearrangements and serendipitious products

Nikolai S. Zefirov; A. S. Koz'min; V. V. Zhdankin; V. N. Kirin; I. V. Bodrikov; B. B. Sedov; V. G. Rau

doi:10.1016/S0040-4039(01)95454-1

Doping-addition of arylsulfenyl chlorides to the tricyclo[4,2,2,0^2,5]deca-3,7,9-triene system: skeletal rearrangements and serendipitious products

Nikolai S. Zefirov
, A. S. Koz'min
, V. V. Zhdankin
, V. N. Kirin
, I. V. Bodrikov
, B. B. Sedov
, V. G. Rau

Chemistry & Biochemistry

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

9 Scopus citations

Abstract

"doping-addition" of 2-NO₂C₆H₄SCl to the tricyclo[4,2,2,0^2,5]deca-3,7,9-triene system {A figure is presented} occurs to give unusual products: (i) rearranged caged cyclopropane {A figure is presented} and (ii) the stable cross-perchlorate {A figure is presented}.

Original language	English (US)
Pages (from-to)	3533-3536
Number of pages	4
Journal	Tetrahedron Letters
Volume	20
Issue number	37
DOIs	https://doi.org/10.1016/S0040-4039(01)95454-1
State	Published - 1979

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@article{6088d977909941209e57f674eda4ee52,

title = "Doping-addition of arylsulfenyl chlorides to the tricyclo[4,2,2,02,5]deca-3,7,9-triene system: skeletal rearrangements and serendipitious products",

abstract = "{"}doping-addition{"} of 2-NO2C6H4SCl to the tricyclo[4,2,2,02,5]deca-3,7,9-triene system \{A figure is presented\} occurs to give unusual products: (i) rearranged caged cyclopropane \{A figure is presented\} and (ii) the stable cross-perchlorate \{A figure is presented\}.",

author = "Zefirov, \{Nikolai S.\} and Koz'min, \{A. S.\} and Zhdankin, \{V. V.\} and Kirin, \{V. N.\} and Bodrikov, \{I. V.\} and Sedov, \{B. B.\} and Rau, \{V. G.\}",

year = "1979",

doi = "10.1016/S0040-4039(01)95454-1",

language = "English (US)",

volume = "20",

pages = "3533--3536",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "37",

}

TY - JOUR

T1 - Doping-addition of arylsulfenyl chlorides to the tricyclo[4,2,2,02,5]deca-3,7,9-triene system

T2 - skeletal rearrangements and serendipitious products

AU - Zefirov, Nikolai S.

AU - Koz'min, A. S.

AU - Zhdankin, V. V.

AU - Kirin, V. N.

AU - Bodrikov, I. V.

AU - Sedov, B. B.

AU - Rau, V. G.

PY - 1979

Y1 - 1979

N2 - "doping-addition" of 2-NO2C6H4SCl to the tricyclo[4,2,2,02,5]deca-3,7,9-triene system {A figure is presented} occurs to give unusual products: (i) rearranged caged cyclopropane {A figure is presented} and (ii) the stable cross-perchlorate {A figure is presented}.

AB - "doping-addition" of 2-NO2C6H4SCl to the tricyclo[4,2,2,02,5]deca-3,7,9-triene system {A figure is presented} occurs to give unusual products: (i) rearranged caged cyclopropane {A figure is presented} and (ii) the stable cross-perchlorate {A figure is presented}.

UR - https://www.scopus.com/pages/publications/49249150476

UR - https://www.scopus.com/pages/publications/49249150476#tab=citedBy

U2 - 10.1016/S0040-4039(01)95454-1

DO - 10.1016/S0040-4039(01)95454-1

M3 - Article

AN - SCOPUS:49249150476

SN - 0040-4039

VL - 20

SP - 3533

EP - 3536

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 37

ER -

Doping-addition of arylsulfenyl chlorides to the tricyclo[4,2,2,0^2,5]deca-3,7,9-triene system: skeletal rearrangements and serendipitious products

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