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Journal article

INTRAMOLECULAR SH2' MACROCYCLIZATIONS

Abstract:: The synthesis of 10-15 membered α-methylene macrocyclic lactones from the functionalised allylstannanes (7e)-(7j) is described. Attempts to synthesise analogous 6-9 membered lactones proved unsuccessful, resulting instead in the production of dilactones and AIBN derived adducts. © 1991.

Publication status:: Published

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APA Style

Baldwin, J., Adlington, R., Mitchell, M., & Robertson, J. (1991). INTRAMOLECULAR SH2' MACROCYCLIZATIONS. TETRAHEDRON, 47(30), 5901–5918.

MLA Style

Baldwin, J., et al. “INTRAMOLECULAR SH2' MACROCYCLIZATIONS.” TETRAHEDRON, vol. 47, no. 30, 1991, pp. 5901–18.

Chicago Style

Baldwin, J, R Adlington, M Mitchell, and J Robertson. 1991. “INTRAMOLECULAR SH2' MACROCYCLIZATIONS.” TETRAHEDRON 47 (30): 5901–18.
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Publisher copy:: 10.1016/S0040-4020(01)86541-8

Authors

+ Baldwin, J More by this author

Role:

Author

+ Adlington, R More by this author

Role:

Author

+ Mitchell, M More by this author

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Author

+ Robertson, J More by this author

Institution:

University of Oxford

Division:

MPLS

Department:

Chemistry

Sub department:

Organic Chemistry

Role:

Author

Bibliographic Details

Journal:: TETRAHEDRON
Volume:: 47
Issue:: 30
Pages:: 5901-5918
Publication date:: 1991-07-22
DOI:: 10.1016/S0040-4020(01)86541-8
ISSN:: 0040-4020

Item Description

Language:: English
Keywords:: SELENIDE

FRAGMENTATION

RADICAL

MACROCYCLIC LACTONE

ALLYLTIN
Pubs id:: pubs:43695
UUID:: uuid:14397fc3-4140-4efb-b394-531d6c660577
Local pid:: pubs:43695
Source identifiers:: 43695
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 1991

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

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