Can I read EPC-syntheses via asymmetric diels-alder reactions/retro diels-alder reactions I: (R)- and (S)-matsutake alcohol. (R)- and (S)-sarcomycin methyl ester on EtoBox?
EPC-syntheses via asymmetric diels-alder reactions/retro diels-alder reactions I: (R)- and (S)-matsutake alcohol. (R)- and (S)-sarcomycin methyl ester by Günter Helmchen; Klaus Ihrig; Heinz Schindler is a Chemistry article available to read on EtoBox.
What is EPC-syntheses via asymmetric diels-alder reactions/retro diels-alder reactions I: (R)- and (S)-matsutake alcohol. (R)- and (S)-sarcomycin methyl ester about?
Enantiomerically pure Diels-Alder adducts, obtained by asymmetric Diels-Alder reaction, were modified diastereoselectively and the products cleaved by retro Diels-Alder reaction to give chiral compounds L(R)-and (S)-I-octen-3-01. (R)-and (S)-sarcomycin methyl ester-1 of high enantiomeric purity.
Who reads EPC-syntheses via asymmetric diels-alder reactions/retro diels-alder reactions I: (R)- and (S)-matsutake alcohol. (R)- and (S)-sarcomycin methyl ester?
It is typically read by researchers, students, and practitioners in Chemistry.
- Author
- Günter Helmchen; Klaus Ihrig; Heinz Schindler
- Publisher
- Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0040-4039)
- Published
- 1987
- Language
- EN
- Field
- Chemistry (Physical Sciences)