Dean R. Bender

Merck & Co., Inc., Rahway, NJ, USA (United States)

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i-10 index

Research Trends

Author Order

Document Type

Co-Authors

Henry Rapoport

Merck & Co., Inc., Rahway, NJ, USA (United States)

A. M. DEMARCO

The Ohio State University Wexner Medical Center

David L. Hughes

University of East Anglia

Paul J. Reider

Princeton University

Daniel R. Knapp

Loyola Marymount University

William R. Leonard

Northwestern University

Kevin M. Belyk

Merck & Co., Inc., Rahway, NJ, USA (United States)

Leonard F. Bjeldanes

University of California, Berkeley

Joseph F. Payack

Bristol-Myers Squibb (United States)

David L. Coffen

Arqule (United States)

Cooperative Institutions

Merck & Co., Inc., Rahway, NJ, USA (United States)

Merck (Japan)

University of California, Berkeley

Stanford University

Merck Institute for Science Education

Lawrence Berkeley National Laboratory

Massanutten Regional Library

MSD (UK) Limited (United Kingdom)

Pfizer (United States)

Heinrich Heine University Düsseldorf

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Selecting appropriate compression for lymphedema patients: American Vein and Lymphatic Society position statement

Phlebology The Journal of Venous Disease (2023)

Heather Hettrick Suzie Ehmann Brandy McKeown Dean R. Bender John Blebea

Lymphedema is a significant and disabling disorder affecting millions of people worldwide. Compression therapy is an important component of lifelong treatment but the specifics of appropriate compression garment selection and prescribing is not always well understood by practitioners and payers.An expert panel of the American Vein and Lymphatic Society was convened to write a Position Statement with explanations and recommendations for the appropriate compression therapy to be used in the treatment of lymphedema patients.A Position Statement was produced by the expert panel with recommendations for documentation and compression therapy treatment. Their recommendations were reviewed, edited, and approved by the Guidelines Committee of the society.This societal Position Statement provides a useful document for reference for medical care providers for the appropriate compression therapy selection and treatment of patients with lymphedema.

Compression Therapy

Position statement

Compression stockings

Statement (logic)

Position (finance)

Position paper

10.1177/02683555221149619

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Citations (4)

Rearrangement of pyruvates to malonates. B-Lactams by ring contraction

The Journal of Organic Chemistry (1973)

Dean R. Bender Leonard F. Bjeldanes Daniel R. Knapp Dennis R. McKean Henry Rapoport

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRearrangement of pyruvates to malonates. B-Lactams by ring contractionD. R. Bender, L. F. Bjeldanes, D. R. Knapp, D. R. McKean, and H. RapoportCite this: J. Org. Chem. 1973, 38, 19, 3439–3440Publication Date (Print):September 1, 1973Publication History Published online1 May 2002Published inissue 1 September 1973https://doi.org/10.1021/jo00959a056RIGHTS & PERMISSIONSArticle Views143Altmetric-Citations8LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (317 KB) Get e-Alerts Get e-Alerts

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10.1021/jo00959a056

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Citations (9)

Synthesis of [O-methyl- 11 C]-2-methoxyethanol by solid phase catalysed addition of N.C.A. [ 11 C]methanol to oxirane.

Journal of Labelled Compounds and Radiopharmaceuticals (1993)

Dean R. Bender K. Hamacher G. Stoecklin

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Citations (0)

Periodate oxidation of .alpha.-keto .gamma.-lactams. Enol oxidation and .beta.-lactam formation. Mechanism of periodate hydroxylation reactions

The Journal of Organic Chemistry (1978)

Dean R. Bender John J. Brennan Henry Rapoport

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTPeriodate oxidation of .alpha.-keto .gamma.-lactams. Enol oxidation and .beta.-lactam formation. Mechanism of periodate hydroxylation reactionsDean R. Bender, John Brennan, and Henry RapoportCite this: J. Org. Chem. 1978, 43, 17, 3354–3362Publication Date (Print):August 1, 1978Publication History Published online1 May 2002Published inissue 1 August 1978https://pubs.acs.org/doi/10.1021/jo00411a020https://doi.org/10.1021/jo00411a020research-articleACS PublicationsRequest reuse permissionsArticle Views560Altmetric-Citations10LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts

Periodate

Beta-lactam

Hydroxylation

Alpha (finance)

Lactam

10.1021/jo00411a020

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Citations (11)

Stereochemistry of .beta.-lactams derived from .alpha.-keto-.gamma.-lactams by ring contraction. X-ray analysis and differential behavior with shift reagents of difunctional .beta.-lactams

The Journal of Organic Chemistry (1975)

Dean R. Bender Henry Rapoport Jon Bordner

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTStereochemistry of .beta.-lactams derived from .alpha.-keto-.gamma.-lactams by ring contraction. X-ray analysis and differential behavior with shift reagents of difunctional .beta.-lactamsDean Bender, Henry Rapoport, and Jon BordnerCite this: J. Org. Chem. 1975, 40, 22, 3208–3213Publication Date (Print):October 1, 1975Publication History Published online1 May 2002Published inissue 1 October 1975https://pubs.acs.org/doi/10.1021/jo00910a009https://doi.org/10.1021/jo00910a009research-articleACS PublicationsRequest reuse permissionsArticle Views64Altmetric-Citations9LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-AlertscloseSupporting Info (1)»Supporting Information Supporting Information Get e-Alerts

Beta-lactam

BETA (programming language)

Lactam

Alpha (finance)

10.1021/jo00910a009

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Citations (10)

ChemInform Abstract: PERIODATE OXIDATION OF α-KETO Γ-LACTAMS. ENOL OXIDATION AND β-LACTAM FORMATION. MECHANISM OF PERIODATE HYDROXYLATION REACTIONS

Chemischer Informationsdienst (1978)

Dean R. Bender James Brennan Henry Rapoport

Abstract Bei der Behandlung mit Periodat entsteht aus dem Keto‐qr‐lactam (I) ein Gemisch der Oxidationsprodukte (II) und (III).

Periodate

Hydroxylation

Lactam

10.1002/chin.197851224

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Citations (0)

Psoralen synthesis. Improvements in furano ring formation. Application to the synthesis of 4,5',8-trimethylpsoralen

The Journal of Organic Chemistry (1979)

Dean R. Bender John E. Hearst Henry Rapoport

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTPsoralen synthesis. Improvements in furano ring formation. Application to the synthesis of 4,5',8-trimethylpsoralenDean R. Bender, John E. Hearst, and Henry RapoportCite this: J. Org. Chem. 1979, 44, 13, 2176–2180Publication Date (Print):June 1, 1979Publication History Published online1 May 2002Published inissue 1 June 1979https://doi.org/10.1021/jo01327a030Request reuse permissionsArticle Views202Altmetric-Citations23LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (732 KB) Get e-Alertsclose Get e-Alerts

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10.1021/jo01327a030

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Citations (24)

Synthesis of the Antifungal β-1,3-Glucan Synthase Inhibitor CANCIDAS (Caspofungin Acetate) from Pneumocandin B₀

The Journal of Organic Chemistry (2007)

William R. Leonard Kevin M. Belyk David A. Conlon Dean R. Bender Lisa DiMichele

A novel three-step synthesis of the highly functionalized antifungal agent CANCIDAS (caspofungin acetate, 2) is described, starting from the natural product pneumocandin B0 (1). The highlights of the synthesis include a stereoselective formation of a phenylthioaminal, a remarkable chemoselective, high-yielding, one-step borane reduction of a primary amide, and a stereoselective substitution of the phenylthioaminal with ethylenediamine producing 2 in a 45% overall yield.

Echinocandins

Boranes

Amide

Natural product

Ethylene diamine

Primary (astronomy)

10.1021/jo062008i

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Citations (35)

ChemInform Abstract: REARRANGEMENT TO PYRUVATES TO MALONATES, BETA‐LACTAMS BY RING CONTRACTION

Chemischer Informationsdienst (1974)

Dean R. Bender Leonard F. Bjeldanes Daniel R. Knapp Dennis R. McKean Henry Rapoport

Abstract 4‐Äthoxycarbonyl‐1‐methyl‐2,3‐pyrrolidindion (I) kann sauer in das 1‐Methyl‐2,3‐ pyrrolidion (II) übergeführt werden.

BETA (programming language)

Beta-lactam

10.1002/chin.197401197

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Citations (0)

Synthetic quinine, analogs. V. Quinolinemethanols related to desvinylquinine

Journal of Heterocyclic Chemistry (1971)

Dean R. Bender David L. Coffen

Abstract Aldol condensation of quinolinecarboxaldehydes with 3‐quinuelidinone followed by acid‐catalyzed hydration of the resulting α,β‐unsalurated ketones provides a short and versatile synthesis of desvinylquinine derivatives. A novel rearrangement of 2‐(9‐phenanthrylmethylene)‐3‐quinuclidinyl earbinols leading to dibenzoindole derivatives is described.

Aldol condensation

Aldol reaction

Quinine

10.1002/jhet.5570080609

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Citations (7)