Journal article

Organolithium-induced synthesis of unsaturated diols from epoxides of dihydrofurans and dihydropyrans

Abstract:: Dihydrofuran and dihydropyran epoxides undergo a stereospecific alkylative double ring-opening with organolithiums to provide a new route to substituted alkenediols.

Publication status:: Published

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APA Style

Hodgson, D., Stent, M., & Wilson, F. (2002). Organolithium-induced synthesis of unsaturated diols from epoxides of dihydrofurans and dihydropyrans. SYNTHESIS-STUTTGART, 10, 1445–1453.

MLA Style

Hodgson, D., et al. “Organolithium-Induced Synthesis of Unsaturated Diols from Epoxides of Dihydrofurans and Dihydropyrans.” SYNTHESIS-STUTTGART, no. 10, 2002, pp. 1445–53.

Chicago Style

Hodgson, D, M Stent, and F Wilson. 2002. “Organolithium-Induced Synthesis of Unsaturated Diols from Epoxides of Dihydrofurans and Dihydropyrans.” SYNTHESIS-STUTTGART, no. 10: 1445–53.
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Publisher copy:: 10.1055/s-2002-33112

Authors

+ Hodgson, D More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Role:: Author

+ Stent, M More by this author

Role:: Author

+ Wilson, F More by this author

Role:: Author

Journal:: SYNTHESIS-STUTTGART More from this journal
Issue:: 10
Pages:: 1445-1453
Publication date:: 2002-08-01
DOI:: 10.1055/s-2002-33112
EISSN:: 1437-210X
ISSN:: 0039-7881

Language:: English
Keywords:: epoxides

diols

alkenes

eliminations

organolithiums
Pubs id:: pubs:38369
UUID:: uuid:5022a8e1-1b07-4757-8aee-30ea54c7c105
Local pid:: pubs:38369
Source identifiers:: 38369
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2002

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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