𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Chiral 2,3-Dihydro-1H-1,3,2-diazaboroles

✍ Scribed by Lothar Weber; Andreas Rausch; Henning B. Wartig; Hans-Georg Stammler; Beate Neumann


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
193 KB
Volume
2002
Category
Article
ISSN
1434-1948

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Preparation, Structure and Reactivity of
✍ Lothar Weber; Eckhard Dobbert; Roland Boese; Michael T. Kirchner; Dieter Bläser 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 386 KB

A series of differently substituted 2-chloro-, 2-fluoro-and 2-with BF 3 •OEt 2 , BCl 3 , or BI 3 in n-hexane. Compounds 3a, 5a, and 5b are also available by sodium amalgam reduction of iodo-2,3-dihydro-1H-1,3,2-diazaboroles have been prepared by various methods. 1,3-Di-tert-butyl-2-fluoro-2,3-dihydr

Synthesis and Structure of 2-Hydro-, 2-A
✍ Lothar Weber; Eckhard Dobbert; Hans-Georg Stammler; Beate Neumann; Roland Boese; 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 303 KB 👁 1 views

1,3,2-diazaborole (4a) and Similarly, 1,3-di-tert-butyl-2-trimethylstannyl-2,3-dihydro-1H-1,3,2-diazaborole (8a) and 1,3-bis(2,6-dimethylphenyl)-2-1,3-bis(2,6-dimethylphenyl)-2,3-dihydro-1H-1,3,2-diazaborole (4b) were formed by the reaction of the corresponding trimethylstannyl-2,3-dihydro-1H-1,3,2-

Synthesis and antimicrobialactivity of 2
✍ D. Srinivasulu; C. Devendranath Reddy; B. Sankar Reddy 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 81 KB 👁 1 views

3, were synthesized by cyclization of 4-propylthio-1,2-phenylenediamine ( 3) with the corresponding dichlorophosphoryl carbamates/thiocarbamates (2a-J) that were obtained by the addition of alcohols/thiols to isocyanatophosphoryl dichloride (1). The structures of the title compounds were confirme

Ab initio molecular orbital study of ene
✍ Freeman, Fillmore; Lee, Choonsun; Po, Henry N.; Hehre, Warren J. 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 228 KB 👁 1 views

Optimized geometries and energies for 3,4-dihydro-1,2-dithiin Ž . Ž . Ž . Ž . 1 , 3,6-dihydro-1,2-dithiin 2 , 4H-1,3-dithiin 3 , and 2,3-dihydro-1,4-dithiin 4 were calculated using ab initio 6-31G U and MP2r6-31G U rr6-31G U methods. At the MP2r6-31G U rr6-31G U level, the half-chair conformer of 4