Tetrahedron Letters

1963

DOI: 10.1016/s0040-4039(01)90770-1

|View full text |Cite

|

Sign up to set email alerts

|

On the base catalyzed cyclization of 2-alkyl-2--toluensulfonoxymethylcyclohexanones

Kenneth B. Wilberg

¹

,

Gerald W. Klein

²

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

Supporting

0

Mentioning

0

Contrasting

0

Year Published

1964

1964

1980

1980

Publication Types

Select...

Article4

Book1

Relationship

Self Cite0

Independent5

Authors

Journals

Cited by 9 publications

References 4 publications

Supporting

0

Mentioning

0

Contrasting

0

Order By: Relevance

Fragmentierungsreaktionen an Carbonylverbindungen mit β‐ständigen elektro‐negativen Substituenten, IV. Hepten‐(6)‐säuren und Bicyclo[3.1.1]‐ bzw. ‐[3.2.0]heptanone‐(6)

¹

,

²

,

³

1967

View full text Add to dashboard Cite

Die Umsetzung alkylsubstituierter Cyclohexanone, 1a–1i, die in β‐Stellung zur Carbonyl‐gruppe Substituenten wie OTs, Halogen oder ⊕N(CH3)3 tragen, mit wäßrig‐alkoholischer Natronlauge liefert neben den durch Fragmentierung entstehenden Hepten‐(6)‐säuren als Haupt‐produkte Bicyclo[3.1.1]‐ und ‐[3.2.0]heptanone‐(6). Die NMR‐Spektren der bicyclischen Ketone gestatten die Zuordnung zur [3.1.1]‐ oder [3.2.0]‐Reihe.

Fragmentierungsreaktionen an Carbonylverbindungen mit β‐ständigen elektro‐negativen Substituenten, IV. Hepten‐(6)‐säuren und Bicyclo[3.1.1]‐ bzw. ‐[3.2.0]heptanone‐(6)

¹

,

²

,

³

1967

View full text Add to dashboard Cite

Die Umsetzung alkylsubstituierter Cyclohexanone, 1a–1i, die in β‐Stellung zur Carbonyl‐gruppe Substituenten wie OTs, Halogen oder ⊕N(CH3)3 tragen, mit wäßrig‐alkoholischer Natronlauge liefert neben den durch Fragmentierung entstehenden Hepten‐(6)‐säuren als Haupt‐produkte Bicyclo[3.1.1]‐ und ‐[3.2.0]heptanone‐(6). Die NMR‐Spektren der bicyclischen Ketone gestatten die Zuordnung zur [3.1.1]‐ oder [3.2.0]‐Reihe.

Steroids cclix11Part CCLVIII. J. Romo, L. Rodriguez-Hahn, P. Joseph-Nathan, M. Martínez and P. Crabbe. Bull. Soc.Chim. France (submitted for publication).. The synthesis of 5β,19 and 6β,19-cyclo steroids

¹

,

²

,

³

et al. 1964

View full text Add to dashboard Cite

No abstract

Rearrangements in Carbanions

1980

Organic Chemistry: A Series of Monographs

View full text Add to dashboard Cite

No abstract

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

hi@scite.ai

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

Henderson, NV 89052, USA

Product

Browser Extension Assistant by scite Citation Statement Search Reference Check Visualizations Dashboards Explore Journals Explore Organizations Explore Funders Embedding Badge Embedding Citation Search Pricing

Resources

Blog Help & FAQ Accessibility Statement API Terms For Universities & Governments For Researchers For Publishers For Corporate, Pharma & Enterprise Author Marketing Become an Affiliate Get an organization trial or quote scite Data & Services

About

News & Press Careers Read our Paper Coverage

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Copyright © 2024 scite LLC. All rights reserved.

Made with 💙 for researchers

Part of the Research Solutions Family.