✦ LIBER ✦

Theoretical studies of the conformational control of additions to bicyclo[m.1.0]Alkan-2-ones. Application and validation of the wizard technique

✍ Scribed by Daniel P. Dolata; David R. Spina

Book ID: 104228471
Publisher: Elsevier Science
Year: 1990
Tongue: French
Weight: 175 KB
Volume: 31
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)97178-8

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Diastereoselective Manipulations of Bicy

Diastereoselective Manipulations of Bicyclo[ m .1.0]alkane Derivatives. 2. Nucleophilic Additions to the Carbonyl Carbons of Bicyclo[ m .1.0]alkan-2-ones 1

✍ Mash, Eugene A.; Gregg, Timothy M.; Kaczynski, Michelle A. 📂 Article 📅 1996 🏛 American Chemical Society 🌐 English ⚖ 310 KB

ChemInform Abstract: Diastereoselective

ChemInform Abstract: Diastereoselective Manipulations of Bicyclo(m.1.0)alkane Derivatives. Part 2. Nucleophilic Additions to the Carbonyl Carbons of Bicyclo(m.1. 0)alkan-2-ones.

✍ E. A. MASH; T. M. GREGG; M. A. KACZYNSKI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB

Theoretical studies on the kinetics of r

Theoretical studies on the kinetics of ring opening of 1-bicyclo[2.1.0]-pentanylmethyl, 1-bicyclo[3.1.0]-hexanylmethyl, and 1-bicyclo[4.1.0]-heptanylmethyl radicals

✍ Han, Ling-Li; Yu, Zhang-Yu; Du, Chun-Mei; Liu, Tao 📂 Article 📅 2014 🏛 Elsevier 🌐 English ⚖ 658 KB

ChemInform Abstract: A Convenient Transf

ChemInform Abstract: A Convenient Transformation of 2-Alkylidenecycloalkanones into Alkyl-Substituted Bicyclo[n.1.0]alkan-1-ols: Application to the Synthesis of Capsaicin.

✍ Dzmitry G. Kananovich; Dzmitry M. Zubrytski; Oleg G. Kulinkovich 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 63 KB 👁 1 views

## Abstract An efficient procedure is developed via conditions A) (formation of β‐iodoketones) followed by conditions B) in the presence of either TmsCl or TiCl(O‐iPr)~3~.

Diastereoselective manipulations of bicy

Diastereoselective manipulations of bicyclo[m.1.0]alkane derivatives. 3. Nucleophilic additions to the carbonyl carbon of (1R,8R)-bicyclo[6.1.0]nonan-2,6-dione2-(2S,3S)-1,4-di-O-methyl-1,2,3,4-butanetetrol ketal

✍ Eugene A. Mash; Kalpana S. Nimkar; James A. Baron 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 776 KB

Conformations of the title compound were studied using a Monte Carlo search technique. Two principal conformational motifs were observed for the bicyclic carbocycle in which both faces of the carbonyl appear susceptible to nucleophilic attack. The title compound was synthesized in eight steps from

Regiospecific additions of hydrazoic aci

Regiospecific additions of hydrazoic acid and benzylamine to 1-(arylsulfonyl)bicyclo[1.1.0]Butanes. Application to the synthesis of cis and trans 2,7-methanoglutamic acids

✍ Yehiel Gaoni 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 263 KB