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The Journal of Organic Chemistry
|
December 4, 2004
Second generation fluorous DEAD reagents have expanded scope in the Mitsunobu reaction and retain convenient separation features
Sivaraman Dandapani, Dennis P Curran
Current Opinion in Chemical Biology
|
April 23, 2010
Current strategies for diversity-oriented synthesis
Sivaraman Dandapani, Lisa A Marcaurelle
Nature Chemical Biology
|
November 17, 2010
Grand challenge commentary: Accessing new chemical space for 'undruggable' targets
Sivaraman Dandapani, Lisa A Marcaurelle
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
June 30, 2004
Separation-friendly Mitsunobu reactions: a microcosm of recent developments in separation strategies
Sivaraman Dandapani, Dennis P Curran
The Journal of Organic Chemistry
|
April 17, 2020
Systematic Investigation of the Scope of Transannular C-H Heteroarylation of Cyclic Secondary Amines for Synthetic Application in Medicinal Chemistry
Zhe Li, Michael Dechantsreiter, Sivaraman Dandapani
Proceedings of the National Academy of Sciences of the United States of America
|
May 26, 2004
Stereoisomer libraries: total synthesis of all 16 stereoisomers of the pine sawfly sex pheromone by a fluorous mixture-synthesis approach
Sivaraman Dandapani, Mario Jeske, Dennis P Curran
The Journal of Organic Chemistry
|
November 5, 2005
Synthesis of all 16 stereoisomers of pinesaw fly sex pheromones--tools and tactics for solving problems in fluorous mixture synthesis
Sivaraman Dandapani, Mario Jeske, Dennis P Curran
Future Medicinal Chemistry
|
December 14, 2012
Hits, leads and drugs against malaria through diversity-oriented synthesis
Sivaraman Dandapani, Eamon Comer, Jeremy R Duvall, et al.
Organic Letters
|
August 24, 2007
Skeletal diversity through radical cyclization of tetrahydropyridine scaffolds
Sivaraman Dandapani, Mihai Duduta, James S Panek, et al.
The Journal of Organic Chemistry
|
August 31, 2011
Diversity-oriented synthesis of 13- to 18-membered macrolactams via ring-closing metathesis
Sivaraman Dandapani, Jason T Lowe, Eamon Comer, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 36) with videos related to
Sort By:
Page
of 4
The Journal of Organic Chemistry
|
December 4, 2004
Second generation fluorous DEAD reagents have expanded scope in the Mitsunobu reaction and retain convenient separation features
Sivaraman Dandapani, Dennis P Curran
Current Opinion in Chemical Biology
|
April 23, 2010
Current strategies for diversity-oriented synthesis
Sivaraman Dandapani, Lisa A Marcaurelle
Nature Chemical Biology
|
November 17, 2010
Grand challenge commentary: Accessing new chemical space for 'undruggable' targets
Sivaraman Dandapani, Lisa A Marcaurelle
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
June 30, 2004
Separation-friendly Mitsunobu reactions: a microcosm of recent developments in separation strategies
Sivaraman Dandapani, Dennis P Curran
The Journal of Organic Chemistry
|
April 17, 2020
Systematic Investigation of the Scope of Transannular C-H Heteroarylation of Cyclic Secondary Amines for Synthetic Application in Medicinal Chemistry
Zhe Li, Michael Dechantsreiter, Sivaraman Dandapani
Proceedings of the National Academy of Sciences of the United States of America
|
May 26, 2004
Stereoisomer libraries: total synthesis of all 16 stereoisomers of the pine sawfly sex pheromone by a fluorous mixture-synthesis approach
Sivaraman Dandapani, Mario Jeske, Dennis P Curran
The Journal of Organic Chemistry
|
November 5, 2005
Synthesis of all 16 stereoisomers of pinesaw fly sex pheromones--tools and tactics for solving problems in fluorous mixture synthesis
Sivaraman Dandapani, Mario Jeske, Dennis P Curran
Future Medicinal Chemistry
|
December 14, 2012
Hits, leads and drugs against malaria through diversity-oriented synthesis
Sivaraman Dandapani, Eamon Comer, Jeremy R Duvall, et al.
Organic Letters
|
August 24, 2007
Skeletal diversity through radical cyclization of tetrahydropyridine scaffolds
Sivaraman Dandapani, Mihai Duduta, James S Panek, et al.
The Journal of Organic Chemistry
|
August 31, 2011
Diversity-oriented synthesis of 13- to 18-membered macrolactams via ring-closing metathesis
Sivaraman Dandapani, Jason T Lowe, Eamon Comer, et al.
Page
of 4