✦ LIBER ✦

ChemInform Abstract: Phosphine-Catalyzed Isomerization-Addition of Oxygen Nucleophiles to 2- Alkynoates.

✍ Scribed by B. M. TROST; C.-J. LI

Book ID: 112021489
Publisher: John Wiley and Sons
Year: 2010
Weight: 31 KB
Volume: 26
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199518049

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Phosphine-Catalyzed Isomerization-Additi

Phosphine-Catalyzed Isomerization-Addition of Oxygen Nucleophiles to 2-Alkynoates

✍ Trost, Barry M.; Li, Chao-Jun 📂 Article 📅 1994 🏛 American Chemical Society 🌐 English ⚖ 240 KB

ChemInform Abstract: Phosphine-Catalyzed

ChemInform Abstract: Phosphine-Catalyzed β′-Umpolung Addition of Nucleophiles to Activated α-Alkyl Allenes.

✍ Tioga J. Martin; Venus G. Vakhshori; Yang S. Tran; Ohyun Kwon 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 69 KB 👁 1 views

ChemInform Abstract: Nucleophilic α-Addi

ChemInform Abstract: Nucleophilic α-Addition to Alkynoates. A Synthesis of Dehydroamino Acids.

✍ B. M. TROST; G. R. DAKE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

ChemInform Abstract: Gold-Catalyzed Addi

ChemInform Abstract: Gold-Catalyzed Addition of Oxygen Nucleophiles to C—C Multiple Bonds

✍ Ross A. Widenhoefer; Feijie Song 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 18 KB 👁 1 views

ChemInform Abstract: Cu-Catalyzed Stereo

ChemInform Abstract: Cu-Catalyzed Stereoselective Conjugate Addition of Arylboronic Acids to Alkynoates.

✍ Yoshihiko Yamamoto; Naohiro Kirai; Yu Harada 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

ChemInform Abstract: Nucleophilic Phosph

ChemInform Abstract: Nucleophilic Phosphine-Catalyzed Iodocyclization of Isoprenoids Bearing an Oxygen Terminal Group.

✍ Akira Sakakura; Gakujun Shomi; Atsushi Ukai; Kazuaki Ishihara 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 45 KB

## Abstract Tbs‐ether of homogeraniol and Tbs‐ester of homogeranic acid are successfully converted to the corresponding iodopolycyclic products in the presence of a catalytic amount of triphenylphosphine with complete diastereoselectivity.