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Journal article

Total synthesis of (-)-nakadomarin A.

Abstract:: A highly diastereoselective bifunctional organocatalyst controlled Michael addition, a nitro-Mannich/lactamization cascade, a furan N-acyliminium cyclisation, a sequential alkyne RCM/syn-reduction and an alkene RCM has allowed a 19 step, highly stereoselective synthesis of (-)-nakadomarin A.

Publication status:: Published

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APA Style

Kyle, A., Jakubec, P., Cockfield, D., Cleator, E., Skidmore, J., & Dixon, D. (2011). Total synthesis of (-)-nakadomarin A. Chemical Communications, 47(36), 10037–10039.

MLA Style

Kyle, A., et al. “Total Synthesis of (-)-Nakadomarin A.” Chemical Communications, vol. 47, no. 36, 2011, pp. 10037–39.

Chicago Style

Kyle, A, P Jakubec, D Cockfield, E Cleator, J Skidmore, and D Dixon. 2011. “Total Synthesis of (-)-Nakadomarin A.” Chemical Communications 47 (36): 10037–39.
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Publisher copy:: 10.1039/c1cc13665h

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+ Kyle, A More by this author

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+ Jakubec, P More by this author

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+ Cockfield, D More by this author

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+ Cleator, E More by this author

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+ Skidmore, J More by this author

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Bibliographic Details

Journal:: Chemical Communications
Volume:: 47
Issue:: 36
Pages:: 10037-10039
Publication date:: 2011-09-01
DOI:: 10.1039/c1cc13665h
EISSN:: 1364-548X
ISSN:: 1359-7345

Item Description

Language:: English
Keywords:: Carbolines

Stereoisomerism

Alkenes

Alkynes

Oxidation-Reduction
Pubs id:: pubs:170109
UUID:: uuid:c416f267-06bf-457c-a726-961172114417
Local pid:: pubs:170109
Source identifiers:: 170109
Deposit date:: 2012-12-19

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Copyright date:: 2011

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

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