Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions

Diego A. Fort; Thomas J. Woltering; Matthias Nettekoven; Henner Knust; Thorsten Bach

doi:10.1039/c3cc40757h

Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions

Diego A. Fort
, Thomas J. Woltering
, Matthias Nettekoven
, Henner Knust
, Thorsten Bach

Chair of Organic Chemistry 1

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

16 Scopus citations

Abstract

Intramolecular [2+2] photocycloaddition reactions of diversely substituted N-Boc protected 4-(allylaminomethyl)-2(5H-furanones resulted in rigid products (53-75%) with three spatially defined positions for further functionalisation.

Original language	English
Pages (from-to)	2989-2991
Number of pages	3
Journal	Chemical Communications
Volume	49
Issue number	29
DOIs	https://doi.org/10.1039/c3cc40757h
State	Published - 14 Mar 2013

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@article{47f25b166725481bbc05da01a288b8e3,

title = "Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions",

abstract = "Intramolecular [2+2] photocycloaddition reactions of diversely substituted N-Boc protected 4-(allylaminomethyl)-2(5H-furanones resulted in rigid products (53-75\%) with three spatially defined positions for further functionalisation.",

author = "Fort, \{Diego A.\} and Woltering, \{Thomas J.\} and Matthias Nettekoven and Henner Knust and Thorsten Bach",

year = "2013",

month = mar,

day = "14",

doi = "10.1039/c3cc40757h",

language = "English",

volume = "49",

pages = "2989--2991",

journal = "Chemical Communications",

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publisher = "Royal Society of Chemistry",

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T1 - Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions

AU - Fort, Diego A.

AU - Woltering, Thomas J.

AU - Nettekoven, Matthias

AU - Knust, Henner

AU - Bach, Thorsten

PY - 2013/3/14

Y1 - 2013/3/14

N2 - Intramolecular [2+2] photocycloaddition reactions of diversely substituted N-Boc protected 4-(allylaminomethyl)-2(5H-furanones resulted in rigid products (53-75%) with three spatially defined positions for further functionalisation.

AB - Intramolecular [2+2] photocycloaddition reactions of diversely substituted N-Boc protected 4-(allylaminomethyl)-2(5H-furanones resulted in rigid products (53-75%) with three spatially defined positions for further functionalisation.

UR - https://www.scopus.com/pages/publications/84875797076

U2 - 10.1039/c3cc40757h

DO - 10.1039/c3cc40757h

M3 - Article

C2 - 23463393

AN - SCOPUS:84875797076

SN - 1359-7345

VL - 49

SP - 2989

EP - 2991

JO - Chemical Communications

JF - Chemical Communications

IS - 29

ER -

Conformationally restricted pyrrolidines by intramolecular [2+2] photocycloaddition reactions

Abstract

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