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Jeffrey A. Robl

Princeton University

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Tetrahedron Letters | 1990

A new and versatile route for the synthesis of highly substituted benzenoids

Jeffrey A. Robl

Abstract A new route for the synthesis of highly substituted benzenoids has been developed. Key steps include the conversion of unsaturated lactone 7 to carboxy substituted cyclohexenone 8 followed aromatization to give phenol 9. The phenolic functionality provides a handle for further modification to give substituted benzenoids of type 2.

Archive | 1995

Quinoline and pyridine anchors for HMG-CoA reductase inhibitors

Jeffrey A. Robl

Archive | 1993

Dual action inhibitors

Donald S. Karanewsky; Joel C. Barrish; Edward W. Petrillo; Jeffrey A. Robl; Denis E. Ryono

Official Gazette of the United States Patent and Trademark Office Patents | 1995

Pyridine anchors for HMG-CoA reductase inhibitors

Jeffrey A. Robl

Archive | 1993

Substituted azepinone dual inhibitors of angiotensin converting enzyme and neutral exdopeptidase

Donald S. Karanewsky; Jeffrey A. Robl

Archive | 1995

Dual action inhibitors containing a pyridazinodiazepine or pyrazolodiazepine lactam ring

Donald S. Karanewsky; Jeffrey A. Robl

Archive | 1996

Acylmercaptoalkanoylamino and mercaptoalkanoylamino benzazepines

Donald S. Karanewsky; Jeffrey A. Robl

Archive | 1997

Mercaptoalkanoylamino and acylmercaptoalkanoylamino benzoxazepines and benzothiazepines

Donald S. Karanewsky; Jeffrey A. Robl

Archive | 1991

PROCESS FOR PREPARING HIGHLY SUBSTITUTED PHENYLS

Jeffrey A. Robl

Archive | 1997

Processes for preparing azepiones useful as intermediates in the preparation of inhibitors of angiotensin converting enzyme and neutral endopeptidase

Jeffrey A. Robl

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Donald S. Karanewsky

Princeton University

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Denis E. Ryono

Princeton University

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Edward W. Petrillo

Princeton University

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Joel C. Barrish

Princeton University

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