cis-5-Amino-6-hydroxycyclohexadiene as a Chiral Building Block: An Asymmetric Synthesis of (−)-Swainsonine

ChemInform Abstract: Synthesis of Optica

ChemInform Abstract: Synthesis of Optically Active 6-Amino-2-cycloheptenone as a Convenient Chiral Building Block for the Preparation of 6-Alkyl-2-cycloheptenone.

✍ Masakazu Koiwa; Georges P.-J. Hareau; Daisuke Morizono; Fumie Sato 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 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

ChemInform Abstract: An Efficient Synthe

ChemInform Abstract: An Efficient Synthesis of Pironetins Employing a Useful Chiral Building Block, (1S,5S,6R)-5-Hydroxybicyclo[4.1.0]heptan-2-one.

✍ Hidenori Watanabe; Hiroyuki Watanabe; Masahiko Bando; Masaru Kido; Takeshi Kitah 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

ChemInform Abstract: A Practical Synthes

ChemInform Abstract: A Practical Synthesis of Nelfinavir, an HIV-Protease Inhibitor, Using a Novel Chiral C4 Building Block: (5R,6S)-2,2-Dimethyl-5-hydroxy-1,3-dioxepan-6-ylammonium Acetate.

✍ Takashi Inaba; Angela G. Birchler; Yasuki Yamada; Shoichi Sagawa; Katsuyuki Yoko 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 39 KB 👁 2 views

ChemInform Abstract: 1,5-Asymmetric Indu

ChemInform Abstract: 1,5-Asymmetric Induction in Addition Reaction of Aldehydes with Chiral Allyltitaniums Having an Amino Group at the Stereogenic Center. Synthesis of Optically Active 2,6-cis-Disubstituted Piperidines.

✍ T. XIN; S. OKAMOTO; F. SATO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 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 Synthesis with 6-tert-Butyl-5

Asymmetric Synthesis with 6-tert-Butyl-5-methoxy-6-methyl-3,6-dihydro-2H-1,4-oxazin-2-one as a New Chiral Glycine Equivalent: Preparation of Enantiomerically Pure α-Tertiary and α-Quaternary α-Amino Acids.

✍ Claus-Juergen Koch; Sona Simonyiova; Joerg Pabel; Annerose Kaertner; Kurt Polbor 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 349 KB 👁 1 views

Asymmetric Synthesis with 6-tert-Butyl-5

Asymmetric Synthesis with 6-tert-Butyl-5-methoxy-6-methyl-3,6-dihydro-2H-1,4-oxazin-2-one as a New Chiral Glycine Equivalent: Preparation of Enantiomerically Pure α-Tertiary and α-Quaternary α-Amino Acids

✍ Claus-Jürgen Koch; Soňa Šimonyiová; Jörg Pabel; Annerose Kärtner; Kurt Polborn; 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 351 KB