✦ LIBER ✦

Reactions of phosphorus compounds. XXVI. Preparation and reactions of 3- and 4-substituted 5-benzoyl-2,2,2,5-tetraphenyl-2-oxaphospholanes

✍ Scribed by Schweizer, Edward Ernest; Creasy, Walter S.

Book ID: 118268026
Publisher: American Chemical Society
Year: 1971
Tongue: English
Weight: 862 KB
Volume: 36
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00815a009

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Reactions of phosphorus compounds. XXI.

Reactions of phosphorus compounds. XXI. Preparation and reactions of 5-benzoyl-2,2,2,5-tetraphenyl-1-oxa-2-phospholane

✍ Schweizer, Edward E.; Creasy, Walter S.; Liehr, Joachim G.; Jenkins, Michael E.; 📂 Article 📅 1970 🏛 American Chemical Society 🌐 English ⚖ 683 KB

Reactions of 3-Thiocyano-2-butanone. I.

Reactions of 3-Thiocyano-2-butanone. I. The Preparation of 2-Substituted-4,5-dimethylthiazoles

✍ Gregory, James T.; Mathes, Roger A. 📂 Article 📅 1952 🏛 American Chemical Society 🌐 English ⚖ 272 KB

Preparation and Grignard reactions of 2-

Preparation and Grignard reactions of 2-benzoyl-4,4-dimethyl-2-oxazoline

✍ Hansen, John F.; Wang, Su. 📂 Article 📅 1976 🏛 American Chemical Society 🌐 English ⚖ 461 KB

Reactions of substituted 5,5-di(R)(Ar)-2

Reactions of substituted 5,5-di(R)(Ar)-2-cyclohexenones. I. SN2 and SN2' reactions of 4-bromoisophorone

✍ Meislich, H.; Jasne, S. 📂 Article 📅 1975 🏛 American Chemical Society 🌐 English ⚖ 740 KB

PREPARATION OF 5-SUBSTITUTED-1,3,4-OXADI

PREPARATION OF 5-SUBSTITUTED-1,3,4-OXADIAZOL-2(3 H )ONES AND THEIR REACTIONS

✍ STEMPEL, ARTHUR.; ZELAUSKAS, JOSEPH.; AESCHLIMANN, JOHN A. 📂 Article 📅 1955 🏛 American Chemical Society 🌐 English ⚖ 441 KB

Stereochemistry of 1,2-Oxaphospholanes,

Stereochemistry of 1,2-Oxaphospholanes, VIII. Synthesis, Stereochemistry, and Ring Opening Reactions of Diastereomeric 3-Hydroxy-2-methoxy-5-methyl-1,2-oxaphospholan-2-ones

✍ Wróblewski, Andrzej E. 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 English ⚖ 511 KB

Addition of dimethyl phosphonate to acetaldol gives a 3 : 7 mixture of diastereomeric dimethyl (1,3-dihydroxybutyl)phosphonates 3 and 4. The relative configurations at C-I and C-3 in these diols were established by the 13C NMR data of their 0-benzylidene derivatives. Axial preference-for the dimetho