Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Qiang Kang

Showing results (1-10 of 153) with videos related to

Pageof 16
Sort By:
Organic Letters|July 31, 2014
Palladium-catalyzed allylic esterification via C-C bond cleavage of a secondary homoallyl alcoholYong Wang, Qiang Kang
Chemical Communications (Cambridge, England)|January 14, 2014
Beijing Symposium 2013: frontiers in organic chemistryQiang Kang, Wenjun Liu
Organic & Biomolecular Chemistry|August 12, 2011
N-heterocyclic carbene-catalyzed aza-Michael additionQiang Kang, Yugen Zhang
Chemical Communications (Cambridge, England)|August 30, 2018
Catalytic asymmetric synthesis of diphenylbutazone analoguesShi-Wu Li, Qiang Kang
Organic Letters|June 9, 2017
Chiral-at-Metal Rh(III) Complex Catalyzed Asymmetric Conjugate Addition of Unactivated Alkenes with α,β-Unsaturated 2-Acyl ImidazolesKuan Li, Qian Wan, Qiang Kang
Journal of Biomolecular Structure & Dynamics|May 28, 2026
mePTL: miRNA-encoded peptides identification using multi-source feature transformation and ensemble learningSiyuan Zhao, Qiang Kang, Lingling Liu
Organic Letters|May 16, 2018
Asymmetric [3 + 2] Cycloaddition Employing N, N'-Cyclic Azomethine Imines Catalyzed by Chiral-at-Metal Rhodium ComplexJun Gong, Qian Wan, Qiang Kang
Frontiers in Human Neuroscience|November 29, 2023
A comprehensive review for machine learning on neuroimaging in obsessive-compulsive disorderXuanyi Li, Qiang Kang, Hanxing Gu
Chemistry, an Asian Journal|May 1, 2018
Enantioselective Mukaiyama-Michael Reaction Catalyzed by a Chiral Rhodium Complex Based on Pinene-Modified Pyridine LigandsJun Gong, Qian Wan, Qiang Kang
Briefings in Bioinformatics|March 30, 2022
RNAI-FRID: novel feature representation method with information enhancement and dimension reduction for RNA-RNA interactionQiang Kang, Jun Meng, Yushi Luan
Pageof 16

Showing results (1-10 of 153) with videos related to

Sort By:
Pageof 16
Organic Letters|July 31, 2014
Palladium-catalyzed allylic esterification via C-C bond cleavage of a secondary homoallyl alcoholYong Wang, Qiang Kang
Chemical Communications (Cambridge, England)|January 14, 2014
Beijing Symposium 2013: frontiers in organic chemistryQiang Kang, Wenjun Liu
Organic & Biomolecular Chemistry|August 12, 2011
N-heterocyclic carbene-catalyzed aza-Michael additionQiang Kang, Yugen Zhang
Chemical Communications (Cambridge, England)|August 30, 2018
Catalytic asymmetric synthesis of diphenylbutazone analoguesShi-Wu Li, Qiang Kang
Organic Letters|June 9, 2017
Chiral-at-Metal Rh(III) Complex Catalyzed Asymmetric Conjugate Addition of Unactivated Alkenes with α,β-Unsaturated 2-Acyl ImidazolesKuan Li, Qian Wan, Qiang Kang
Journal of Biomolecular Structure & Dynamics|May 28, 2026
mePTL: miRNA-encoded peptides identification using multi-source feature transformation and ensemble learningSiyuan Zhao, Qiang Kang, Lingling Liu
Organic Letters|May 16, 2018
Asymmetric [3 + 2] Cycloaddition Employing N, N'-Cyclic Azomethine Imines Catalyzed by Chiral-at-Metal Rhodium ComplexJun Gong, Qian Wan, Qiang Kang
Frontiers in Human Neuroscience|November 29, 2023
A comprehensive review for machine learning on neuroimaging in obsessive-compulsive disorderXuanyi Li, Qiang Kang, Hanxing Gu
Chemistry, an Asian Journal|May 1, 2018
Enantioselective Mukaiyama-Michael Reaction Catalyzed by a Chiral Rhodium Complex Based on Pinene-Modified Pyridine LigandsJun Gong, Qian Wan, Qiang Kang
Briefings in Bioinformatics|March 30, 2022
RNAI-FRID: novel feature representation method with information enhancement and dimension reduction for RNA-RNA interactionQiang Kang, Jun Meng, Yushi Luan
Pageof 16