Nitro-olefin trapping reaction of enolates generated by conjugate addition reaction: short syntheses of PGE1, 6-Oxo-PGE1, 6-Oxo-PGF1α, and PGI2-Reference-Cited by-同舟云学术

Nitro-olefin trapping reaction of enolates generated by conjugate addition reaction: short syntheses of PGE1, 6-Oxo-PGE1, 6-Oxo-PGF1α, and PGI2

Published:1987-01 Issue:5 Volume:43 Page:813-824
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Tanaka Toshio,Hazato Atsuo,Bannai Kiyoshi,Okamura Noriaki,Sugiura Satoshi,Manabe Kenji,Toru Takeshi,Kurozumi Seizi,Suzuki Masaaki,Kawagishi Toshio,Noyori Ryoji

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference75 articles.

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2. Prostaglandin synthesis. 12. Synthesis of (7E)- and (7Z)-punaglandin 4. Structural revision

3. Organocopper Conjugate Addition-Enolate Trapping Reactions

4. Utilization of magnesium enolates in the Michael reaction

5. Conjugate addition-annelation. Highly regiospecific and stereospecific synthesis of polycyclic ketones

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