𝔖 Bobbio Scriptorium

✦ LIBER ✦

Software aid for mask shop : N. N. Kundu and S. N. Gupta. Microelectron. J.16 (6), 7 (1985)

Book ID: 103284074
Publisher: Elsevier Science
Year: 1987
Tongue: English
Weight: 122 KB
Volume: 27
Category: Article
ISSN: 0026-2714
DOI: 10.1016/0026-2714(87)90697-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Defects in photomasks : S. N. Gupta, A.

Defects in photomasks : S. N. Gupta, A. K. Bagchi and N. N. Kundu. Microelectron. J. 16 1 22 (1985)

📂 Article 📅 1986 🏛 Elsevier Science 🌐 English ⚖ 131 KB

Computation of optical image profile for

Computation of optical image profile for lithography and linewidth measurement : N. N. Kundu, B. P. Mathur and S. N. Gupta. Microelectron. J.17(6), 14 (1986)

📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 129 KB

A data-base for IC mask making : N. N. K

A data-base for IC mask making : N. N. Kundu, S. N. Gupta, A. K. Bagchi, D. R. Nagpal, A. V. Ramani and W. S. Khokle. Microelectron. J.14 (5), 43 (1983)

📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 132 KB

A data-base for IC mask making: N.N. Kun

A data-base for IC mask making: N.N. Kundu, S.N. Gupta, A.K. Bagchi, D.R. Nagpal, A.V. Ramani and W.S. Khokle Microelectron. J. 14 (5), 43 (1983)

📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 104 KB

A simple expert system for a mask shop :

A simple expert system for a mask shop : S. N. Gupta and K. I. Arshak. Microelectron. J.18(4), 35 (1987)

📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 123 KB

Design and synthesis of potent N1-substi

Design and synthesis of potent N1-substituted indole melatonin receptor agonistsSelected data for 15: 1H NMR (200 MHz, CDCl3) δ 0.87–0.92 (t, 3H, CH3CH2, J = 7.3) 1.58–1.63 (quintet, 2H, CH2CH2CO, J = 7.3), 2.06–2.10 (t, 2H, CH2CO, J = 7.3) 2.86–2.89 (t, 2H, ArCH2, J = 6.8), 3.53–3.58 (q, 2H, CH2NH, J = 6.5), 3.83 (s, 3H, CH3O) 4.01 (s, 3H, CH3ON), 5.48 (br s, 1H, NHCO), 6.88–7.30 (m, 4H, Harom); 13C NMR (50 MHz, CDCl3) δ 13.7, 19.1, 25.3, 38.8, 39.4, 55.9, 65.7, 100.8, 108.6, 109.4, 112.9, 121.8, 122.7, 124.3, 154.5, 172.9. Anal. (C16H22N2O3) C, H, N.

✍ Tsotinis, Andrew; Eleutheriades, Andreas; Hough, Katherine; Sugden, David 📂 Article 📅 2003 🏛 Royal Society of Chemistry 🌐 English ⚖ 100 KB