A new synthesis of chlorins has been developed, based upon the acid-catalyzed .... quantities of formyl derivative 15a by oxidation with SeO2.17 Unexpectedly, ...
Peter A. Jacobi*, Sandra Lanz, Indranath Ghosh, Sam H. Leung, Franziska Lower, and Douglas Pippin. Org. Lett. , 2001, 3 (19), pp 3061â3061. DOI: 10.1021/ ...
Studies in Chlorin Chemistry. 3. A Practical Synthesis of C,D-Ring Symmetric Chlorins of Potential Utility in Photodynamic Therapy. William G. O'Neal, William P.
Volume 3, 2001. Peter A. Jacobi,* Sandra Lanz, Indranath Ghosh,. Sam H. Leung, Franziska Lower, and Douglas Pippin. A New Synthesis of Chlorins. Page 834 ...
Feb 21, 2001 - Peter A. Jacobi , Sandra Lanz , Indranath Ghosh , Sam H. Leung , Franziska Loewer , Douglas Pippin. ChemInform 2001 32 (29), no-no ...
2001 American Chemical Society. Published on Web 02/21/2001. Page 2. Not surprisingly, porphyrins are the easiest of the mac- rocyclic tetrapyrroles to prepare, since the ring itself ... Br). Bilatrienes 5, in turn, are constructed from monocyclic bu
Dec 10, 2003 - Enantioselective Synthesis of (+)-Isolysergol via Ring-Closing Metathesis. Jason A. Deck and Stephen F. Martin. Organic Letters 2010 12 (11), 2610-2613. Abstract | Full Text HTML | PDF | PDF w/ Links. Cover Image ...
Interest in the chemistry of aromatic pentafluorosulfanyl compounds was briefly ... 3-Nitropentafluorosulfanylbenzene, 5, had been obtained earlier by direct ...
6, 14, 2417-2419 ... The elimination of HCl from SF5Cl adducts of simple alkenes has been achieved ... The best results were achieved using sodium ethoxide.
3 days ago - Consequently, it is the go-to, one-stop journal where researchers can reliably expect to find a richly dense collection of first-class organic ...
ORGANIC LETTERS 2001 Vol. 3, No. 19 3061
Additions and Corrections
Volume 3, 2001
Vol. 3, 2001
Peter A. Jacobi,* Sandra Lanz, Indranath Ghosh, Sam H. Leung, Franziska Lower, and Douglas Pippin
Zihong Guo,* Antoulinakis
A New Synthesis of Chlorins.
Preparation and Photochemical Rearrangements of 2-Phenyl-2,5-cyclohexadien-1-ones. An Efficient Route to Highly Substituted Phenols.
Page 834, Compound identification was omitted from Table 1 during preparation for publication. See below for the complete version of Table 1.
Table 1. Summary of Yieldsa
Arthur
10.1021/ol0165490 Published on Web 08/24/2001
12
13
17
19
2019
7
a b c d
96% 98% 85% 74%
68% 89% 75% 76%
99% 91% 86% 49%
68% 68% 71% 41%
62% 71% 73% 57%
99% 68% 62% 99%
a
Compound numbers correspond to Schemes 1-3.
OL16540Y 10.1021/ol016540y Published on Web 08/16/2001
Schultz,
and
Evan
G.
Page 1177, an additional author, Evan G. Antoulinakis, has been added to this paper. Also, the Acknowledgment should read “We thank Dr. Kshitij Thakkar for his initial contributions in the development of the chemistry in Schemes 2 and 5 and other relevant work and Dr. Nalin Subasinghe for helpful discussions.” OL0165490
