𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of olivetol-4,6−14C2, and its conversion to (–)–δ9-6a, 10a-trans-tetrahydrocannabinol-2,4−14C2 via (–)–Δ8-6a, 10a-trans-tetrahydrocannabinol-2,4−14C2

✍ Scribed by A. A. Liebman; D. H. Malarek; A. M. Dorsky; H. H. Kaegi


Publisher
John Wiley and Sons
Year
1971
Tongue
French
Weight
311 KB
Volume
7
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


A facile micromolar reduction of [1,2,3,
✍ Neil J. Lewis; Frederick D. Cazer 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 French ⚖ 118 KB

## Abstract The preparation of 6,7‐dihydro[1,2,3,4,10‐^14^C]aldrin is reported by catalytic reduction of [1,2,3,4,10‐^14^C]aldrin. Modification of previously published conditions afforded the desired product in 97.1% yield as assayed by electron capture gas chromatography. The convenient one vessel

One step conversion of glutarimide-2,6-1
✍ L. H. McKendry 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 French ⚖ 208 KB

## Abstract A convenient method of preparing 2‐octyl (4‐amino‐3,5‐dichloro‐6‐fluoro‐2‐pyridinyloxy‐2,6‐^14^C)acetate from glutarimide‐2,6‐^14^C is described. The process includes a novel one‐step conversion of glutarimide‐2,6‐^14^C to pentachloropyridine‐2,6‐^14^C.

The synthesis of (−)-4-methyl-8-chloro-t
✍ Fengjiun Kuo; William J. Wheeler 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 French ⚖ 340 KB

## Abstract The synthesis of the C‐14 labeled isotopomer of LY300502, a potent 5α‐reductase inhibitor has been accomplished in four radiochemical steps. The route involves the synthesis of LY300502‐[^14^C] from LY300502 __via__ a circuitous route; the label was introduced with ethyl chloroformate‐[

Facile preparation of a 4-substituted [2
✍ J. Richard Heys; A. J. Villani; A. R. Mastrocola 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 French ⚖ 437 KB 👁 1 views

14ClFormaldehyde was used in a nucleophile-assisted iminium ion cyclization with N-benzyl-3-butynylamine to provide N-benzyl-4-iodo-I ,2,5,6-tetrahydr0[2,6-1~C2]pyridine. Palladium-catalyzed coupling of this vinyl iodide with the organozinc derivative 2 gave the corresponding 4arylated tetrahydropyr