✦ LIBER ✦

Synthesis of Highly Functionalized Amino Acid and Hydroxy Acid Derivatives from γ-Aminoalkyl-Substituted α-Methylene-γ-butyrolactones

✍ Scribed by Steffen Steurer; Joachim Podlech

Publisher: John Wiley and Sons
Year: 2002
Tongue: English
Weight: 641 KB
Volume: 2002
Category: Article
ISSN: 1434-193X
DOI: 10.1002/1099-0690(200203)2002:5<899::aid-ejoc899>3.0.co;2-#

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis of Highly

ChemInform Abstract: Synthesis of Highly Functionalized Amino Acid and Hydroxy Acid Derivatives from γ-Aminoalkyl-Substituted α-Methylene-γ-butyrolactones.

✍ Steffen Steurer; Joachim Podlech 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 43 KB 👁 2 views

ChemInform Abstract: 1,4-Additions to γ-

ChemInform Abstract: 1,4-Additions to γ-Aminoalkyl-Substituted α-Methylene γ-Butyrolactones: Synthesis of Highly Functionalized Amino Acid Derivatives.

✍ Steffen Steurer; Joachim Podlech 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Aminoalkyl-Substituted α-Methylene-γ-but

Aminoalkyl-Substituted α-Methylene-γ-butyrolactones from α-Amino Acids Using an Indium-Mediated Barbier Allyl Addition

✍ Steffen Steurer; Joachim Podlech 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 398 KB 👁 1 views

The indium-mediated reaction of Z-protected α-amino transformation of the amino aldehydes. Acid-catalyzed esterification (H 2 SO 4 in Et 2 O) led to α-methylene-γaldehydes 1-6 with 2-(bromomethyl)acrylates 8/9 in aqueous solvents has been investigated. The preference for the butyrolactones 17-22 wit

ChemInform Abstract: Aminoalkyl-Substitu

ChemInform Abstract: Aminoalkyl-Substituted α-Methylene-γ-butyrolactones from α-Amino Acids Using an Indium-Mediated Barbier Allyl Addition.

✍ Steffen Steurer; Joachim Podlech 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

Aminoalkyl-Substituted α-Methylene-γ-butyrolactones from α-Amino Acids Using an Indium-Mediated Barbier Allyl Addition. α-Amino aldehydes, prepared from α-amino acids, can be cleanly transformed into esters of type (III) in high yields and without racemization by In-induced Barbier reaction. The di

ChemInform Abstract: Highly Stereoselect

ChemInform Abstract: Highly Stereoselective Synthesis of Spiro-α-methylene-γ-butyrolactones: The Role of α-Hydroxy Substitution.

✍ M. S. SAWANT; R. KATOCH; G. K. TRIVEDI; U. R. DESAI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 39 KB 👁 1 views

ChemInform Abstract: Facile Stereoselect

ChemInform Abstract: Facile Stereoselective Synthesis of γ-Substituted γ-Amino Acids from the Corresponding α-Amino Acids.

✍ M. SMRCINA; P. MAJER; E. MAJEROVA; T. A. GUERASSINA; M. A. EISSENSTAT 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Facile Stereoselective Synthesis of γ-Substituted γ-Amino Acids from the Corresponding α-Amino Acids. -The mild and short procedure presented is compatible with common side-chain protecting groups, sensitive functionalities and preserves the chirality of the starting α-amino acid.