✦ LIBER ✦

Asymmetric Diels-Alder reaction: applications of chiral dienophiles

✍ Scribed by Masamune, Satoru; Reed, Lawrence A.; Davis, Jeffrey T.; Choy, William

Book ID: 118209529
Publisher: American Chemical Society
Year: 1983
Tongue: English
Weight: 505 KB
Volume: 48
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00171a072

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Asymmetric Diels-Alder reaction: design

Asymmetric Diels-Alder reaction: design of chiral dienophiles

✍ Choy, William; Reed, Lawrence A.; Masamune, Satoru 📂 Article 📅 1983 🏛 American Chemical Society 🌐 English ⚖ 413 KB

Asymmetric Diels-Alder Cycloadditions wi

Asymmetric Diels-Alder Cycloadditions with Chiral Carbamoyl Dienophiles

✍ Albert Defoin; Agnès Brouillard-Poichet; Jacques Streith 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 German ⚖ 873 KB

Asymmetric Diels–Alder Reactions with Ch

Asymmetric Diels–Alder Reactions with Chiral Acetylenic Carbene Complexes as Dienophiles

✍ Annette Rahm; Arnold L. Rheingold; William D. Wulff 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 267 KB

AbstractÐA new synthetic method is developed for the asymmetric Diels±Alder reactions of acetylenic dienophiles. Acetylenic Fischer carbene complexes with chiral pyrrolidines as the heteroatom stabilizing substituent were anticipated to block three of the four possible approaches of a diene and lead

Asymmetric Diels-Alder reactions of carb

Asymmetric Diels-Alder reactions of carboxylic ester dienophiles promoted by chiral Lewis acids

✍ Devine, Paul N.; Oh, Taeboem 📂 Article 📅 1992 🏛 American Chemical Society 🌐 English ⚖ 515 KB

ChemInform Abstract: Asymmetric Diels—Al

ChemInform Abstract: Asymmetric Diels—Alder Reactions with Chiral Acetylenic Carbene Complexes as Dienophiles.

✍ Annette Rahm; Arnold L. Rheingold; William D. Wulff 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Asymmetric induction of four chiral cent

Asymmetric induction of four chiral centers by hetero Diels-Alder reaction of a chiral nitroso dienophile

✍ Werbitzky, Oleg ;Klier, Konrad ;Felber, Helena 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 371 KB

## Abstract The Diels‐Alder reaction of __cis__‐5,6‐diacetoxy‐1,3‐cyclohexadiene (1), which has a __meso__ configuration, with the chiral nitroso dienophile 2 occurs with induction of four asymmetric centers in very high optical yield (ee = 94%) and leads to the dihydro oxazine 3 (89%). The influen