✦ LIBER ✦

Diastereoselective Silacyclopropanations of Functionalized Chiral Alkenes

✍ Scribed by Driver, Tom G.; Franz, Annaliese K.; Woerpel, K. A.

Book ID: 127172099
Publisher: American Chemical Society
Year: 2002
Tongue: English
Weight: 47 KB
Volume: 124
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja020183k

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Diastereoselective Silacyclopropanations

Diastereoselective Silacyclopropanations of Functionalized Chiral Alkenes.

✍ Tom G. Driver; Annaliese K. Franz; K. A. Woerpel 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 42 KB

Regio- and Diastereoselective Cu-Mediate

Regio- and Diastereoselective Cu-Mediated Trifluoromethylation of Functionalized Alkenes

✍ Besset, Tatiana; Cahard, Dominique; Pannecoucke, Xavier 📂 Article 📅 2013 🏛 American Chemical Society 🌐 English ⚖ 511 KB

Metal-Catalyzed Silacyclopropanation of

Metal-Catalyzed Silacyclopropanation of Mono- and Disubstituted Alkenes.

✍ Jelena Cirakovic; Tom G. Driver; K. A. Woerpel 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Metal-Catalyzed Silacyclopropanation of

Metal-Catalyzed Silacyclopropanation of Mono- and Disubstituted Alkenes

✍ Ćiraković, Jelena; Driver, Tom G.; Woerpel, K. A. 📂 Article 📅 2002 🏛 American Chemical Society 🌐 English ⚖ 41 KB

Diastereoselective Synthesis of Fullerop

Diastereoselective Synthesis of Fulleropyrrolidines from Suitably Functionalized Chiral Cyclobutanes

✍ Illescas, Beatriz M.; Martín, Nazario; Poater, Jordi; Solà, Miquel; Aguado, Gemm 📂 Article 📅 2005 🏛 American Chemical Society 🌐 English ⚖ 185 KB

Diastereoselective [3+2]-photocycloaddit

Diastereoselective [3+2]-photocycloaddition of chiral 1,4-naphthalenedicarboxylic esters to alkenes

✍ Yasuo Kubo; Masahiro Yoshioka; Satoshi Nakajima; Isamu Inamura 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 216 KB

3+2]-Photocycloaddition of di-(-)-menthyl, di-(-)-8-phenylmenthyl, and di-(-)-bornyl 1,4naphthalenedicarboxylates to alkenes, such as isobutene, styrene, and ~-methylstyrene, proceeded with diastereoselectivity, up to 62% diastereomeric excess (de), largely depending on the concavity of the auxiliar