Journal article

A SHORT AND EFFICIENT SYNTHESIS OF THE C-3 TO C-10 PORTION OF THE MAYTANSINOIDS

Abstract:: The cyclic carbamate (3), a key intermediate in our projected synthesis of trenudine (2), has been synthesised from 3,4-epoxycyclohexene (4) by ozonolytic cleavage of the cyclopentene (9) as a key step. © 1991.

Publication status:: Published

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APA Style

Hodgson, D., Parsons, P., & Stones, P. (1991). A SHORT AND EFFICIENT SYNTHESIS OF THE C-3 TO C-10 PORTION OF THE MAYTANSINOIDS. TETRAHEDRON, 47(24), 4133–4142.

MLA Style

Hodgson, D, et al. “A SHORT AND EFFICIENT SYNTHESIS OF THE C-3 TO C-10 PORTION OF THE MAYTANSINOIDS.” TETRAHEDRON, vol. 47, no. 24, 1991, pp. 4133–42.

Chicago Style

Hodgson, D, P Parsons, and P Stones. 1991. “A SHORT AND EFFICIENT SYNTHESIS OF THE C-3 TO C-10 PORTION OF THE MAYTANSINOIDS.” TETRAHEDRON 47 (24): 4133–42.
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Publisher copy:: 10.1016/S0040-4020(01)86450-4

Authors

+ Hodgson, D More by this author

Role:: Author

+ Parsons, P More by this author

Role:: Author

+ Stones, P More by this author

Role:: Author

Journal:: TETRAHEDRON More from this journal
Volume:: 47
Issue:: 24
Pages:: 4133-4142
Publication date:: 1991-06-10
DOI:: 10.1016/S0040-4020(01)86450-4
ISSN:: 0040-4020

Language:: English
Pubs id:: pubs:52156
UUID:: uuid:23580e01-f171-4110-8042-8f7430913e9d
Local pid:: pubs:52156
Source identifiers:: 52156
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_23580e01f171411080428f7430913e9d

Terms of use

Copyright date:: 1991

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

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