Synthetic Communications
 2014
DOI: 10.1080/00397911.2014.930494
|View full text |Cite
|
Sign up to set email alerts
|

Investigation of the Mitsunobu Reaction of BINOL and Cinchona Alkaloids: Inversion or Retention of Configuration?

Wei Yang
1
,
Yuming Cui
2
,
Jingfeng Zou
3
et al.
Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2015
2015
2019
2019

Publication Types

Select...
2
1

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 45 publications
0
1
0
Order By: Relevance
“…41 This functional includes long range and dispersion corrections and the accuracy of this method has been tested for similar systems in our previous studies. 29,42,43 The (75 302) integration grid was applied in all cases. The geometries of the catalysts were optimised both in the gas phase and in ethyl acetate solvent using SM8 continuum solvation method.…”
Section: Generalmentioning
confidence: 99%

New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis

Nagy
1
,
Gyula
2
,
Kisszékelyi
3
et al. 2019
New J. Chem.
16
0
16
0
View full textAdd to dashboardCite
show abstract
“…41 This functional includes long range and dispersion corrections and the accuracy of this method has been tested for similar systems in our previous studies. 29,42,43 The (75 302) integration grid was applied in all cases. The geometries of the catalysts were optimised both in the gas phase and in ethyl acetate solvent using SM8 continuum solvation method.…”
Section: Generalmentioning
confidence: 99%

New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis

Nagy
1
,
Gyula
2
,
Kisszékelyi
3
et al. 2019
New J. Chem.
16
0
16
0
View full textAdd to dashboardCite
show abstract

Cinchona Alkaloids—Derivatives and Applications

Boratyński
1
,
Zielińska-Błajet
2
,
Skarżewski
3
2019
The Alkaloids: Chemistry and Biology
48
0
36
0
View full textAdd to dashboardCite

l-Proline derived arylmethanamine ligands and their application in the copper-catalyzed asymmetric Henry reaction: a rare example of a Cu-complex with a dicopper tetraacetate core

Niedziejko
1
,
Szewczyk
2
,
Kalicki
3
et al. 2015
Tetrahedron: Asymmetry
16
0
4
0
View full textAdd to dashboardCite
scite logo

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

customersupport@researchsolutions.com

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

Product
Browser ExtensionAssistant by sciteCitation Statement SearchReference CheckVisualizationsDashboardsExplore JournalsExplore OrganizationsExplore FundersEmbedding BadgeEmbedding Citation SearchPricing
Resources
BlogHelp & FAQAccessibility StatementAPI TermsFor Universities & GovernmentsFor ResearchersFor PublishersFor Corporate, Pharma & EnterpriseAuthor MarketingBecome an AffiliateGet an organization trial or quotescite Data & Services
About
News & PressCareersRead our PaperCoverage

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

BlogTerms and ConditionsAPI TermsPrivacy PolicyContactCookie PreferencesDo Not Sell or Share My Personal Information

Copyright © 2025 scite LLC. All rights reserved.

Made with 💙 for researchers

Part of the Research Solutions Family.